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AbbVie Contract Manufacturing
FDA Orange Book

Abbvie Contract Manufacturing-PSE

Success Factors for Pre-Filled Syringe CMO Selection

15 Jul 2024

// PRESS RELEASE

AbbVie Preps Global Parenteral Sites For Annex 1 Compliance Requirements

24 Jun 2024

// PRESS RELEASE

Translating Environmental, Social and Governance (ESG) Benefits to our Partners

10 May 2024

// PRESS RELEASE

Data Compilation
#PharmaFlow

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Latest Content by PharmaCompass

https://www.youtube.com/embed/z4lt1f6ZXL4

AbbVie Contract Manufacturing

VISIT THE VIRTUAL BOOTH, Contact Details

VISIT THE VIRTUAL BOOTH
Review portfolio & marketing content
CONTACT DETAILS
Google Map, LinkedIn, Emails...

EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

PRESENTATION(s)

Corporate Presentation, GMP Certificate 2025, Aseptic Fill-Finish: Vial, Custom Active Pharmaceutical Ingredient, Opthalmics, Topical, Oral Solid Dose, Hot Melt Extrusion, Biologics Development & Drug Substance Manufacturing, Antibody Drug Conjugates (ADC), Product List 2025, Potent API and Drug Product, Fill-Finish: PreFilled Syringe, Our Impact 2019, AbbVie Global Supply Chain Management

Corporate Presentation
GMP Certificate 2025
Aseptic Fill-Finish: Vial
Custom Active Pharmaceutical Ingredient
Opthalmics
Topical
Oral Solid Dose
Hot Melt Extrusion
Biologics Development & Drug Substance Manufacturing
Antibody Drug Conjugates (ADC)
Product List 2025
Potent API and Drug Product
Fill-Finish: PreFilled Syringe
Our Impact 2019
AbbVie Global Supply Chain Management

VIDEO(s)

Corporate Video, Biopharmaceutical Contract Manufacturing Facility, Eye Care Ophthalmic Contract Manufacturing Facility, Fill Finish State of The Art Manufacturing Facility, We are AbbVie, Biologics Ballytivnan, Bioresearch Center Overview, Filling Suite, Harvest Setup, Logistics: Shipping Bottles, Microbiology Testing, POD Filter Disassembly, Water for Injection (WFI) Still, Weigh/Dispense, Introducing AbbVie, Our Principles

Corporate Video
Biopharmaceutical Contract Manufacturing Facility
Eye Care Ophthalmic Contract Manufacturing Facility
Fill Finish State of The Art Manufacturing Facility
We are AbbVie
Biologics Ballytivnan
Bioresearch Center Overview
Filling Suite
Harvest Setup
Logistics: Shipping Bottles
Microbiology Testing
POD Filter Disassembly
Water for Injection (WFI) Still
Weigh/Dispense
Introducing AbbVie
Our Principles

DIGITAL CONTENT

31 Corporate Content #SupplierSpotlight, 1 Data Compilation #PharmaFlow, 47 News #PharmaBuzz

31 Corporate Content #SupplierSpotlight
1 Data Compilation #PharmaFlow
47 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

25 All APIs, 7 USDMF, 6 CEP/COS, 7 KDMF, 7 NDC API, 8 Listed APIs

25 All APIs
7 USDMF
6 CEP/COS
7 KDMF
7 NDC API
8 Listed APIs

DEVELOPMENTS

1512 Drugs in Development

1512 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1197 FDF Dossiers, 411 FDA Orange Book, 355 Europe, 130 Canada, 233 Australia, 68 South Africa

1197 FDF Dossiers
411 FDA Orange Book
355 Europe
130 Canada
233 Australia
68 South Africa

SERVICES

API Manufacturing, Drug Product Manufacturing, API & Drug Product Development, Packaging

API Manufacturing
Drug Product Manufacturing
API & Drug Product Development
- 1 Preformulation & Material Science
- 6 Formulation Development
Packaging
- 2 Contract Services

KEY SERVICES

Ophthalmic Solution Manufacturing, Prefilled Syringe Contract Manufacturing, Ophthalmic Formulation Development, Parenteral Formulation Development, Topical Formulation Development, Development of Topical Creams & Gels, Aseptic Fill & Finish Services

Ophthalmic Solution Manufacturing
Prefilled Syringe Contract Manufacturing
Ophthalmic Formulation Development
Parenteral Formulation Development
Topical Formulation Development
Development of Topical Creams & Gels
Aseptic Fill & Finish Services

REF. STANDARDS & IMPURITIES

1 Others

1 Others

INSPECTIONS & REGISTRATIONS

104 FDA, 51 EDQM, 4 GDUFA

104 FDA
51 EDQM
4 GDUFA

Xls

Filters

Reset all filters

Filters

FILTER :

filter Active Ingredients Reset all filters

411 All

01 3ACETAMINOPHEN; HYDROCODONE BITARTRATE

02 1ACYCLOVIR SODIUM

03 2ADALIMUMAB

04 1ALCAFTADINE

05 3ASENAPINE MALEATE

06 2ASPIRIN; BUTALBITAL; CAFFEINE

07 1ASPIRIN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE

08 3ATOGEPANT

09 1ATROPINE

10 3ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE

11 1AVIBACTAM SODIUM; AZTREONAM

12 1AVIBACTAM SODIUM; CEFTAZIDIME

13 1BERACTANT

14 4BIMATOPROST

15 1BIPERIDEN HYDROCHLORIDE

16 1BIPERIDEN LACTATE

17 4BRIMONIDINE TARTRATE

18 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE

19 2CALCITRIOL

20 1CARBIDOPA; LEVODOPA

21 4CARIPRAZINE HYDROCHLORIDE

22 3CARTEOLOL HYDROCHLORIDE

23 3CEFDINIR

24 2CEFTAROLINE FOSAMIL

25 2CHLORAMPHENICOL

26 1CHLORAMPHENICOL; PREDNISOLONE

27 2CHOLINE FENOFIBRATE

28 3CISATRACURIUM BESYLATE

29 4CITALOPRAM HYDROBROMIDE

30 8CLARITHROMYCIN

31 1CROMOLYN SODIUM

32 7CYCLOSPORINE

33 1DALBAVANCIN HYDROCHLORIDE

34 2DARIFENACIN HYDROBROMIDE

35 1DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR

36 1DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR

37 1DEOXYCHOLIC ACID

38 2DESERPIDINE

39 3DESERPIDINE; HYDROCHLOROTHIAZIDE

40 2DEXAMETHASONE

41 4DEXTROTHYROXINE SODIUM

42 3DICUMAROL

43 4DICYCLOMINE HYDROCHLORIDE

44 3DILTIAZEM HYDROCHLORIDE

45 1DIPIVEFRIN HYDROCHLORIDE

46 8DIVALPROEX SODIUM

47 4DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE

48 1DOXACURIUM CHLORIDE

49 1EFLORNITHINE HYDROCHLORIDE

50 2ELAGOLIX SODIUM

51 1ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM

52 2ELUXADOLINE

53 1EPINASTINE HYDROCHLORIDE

54 3EPROSARTAN MESYLATE

55 2EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE

56 4ESCITALOPRAM OXALATE

57 5ESTRADIOL

58 4ETHCHLORVYNOL

59 4ETHINYL ESTRADIOL; NORETHINDRONE

60 1ETHOXZOLAMIDE

61 1FAMOTIDINE

62 8FENOFIBRATE

63 4FLUOCINOLONE ACETONIDE

64 3FLUOROMETHOLONE

65 1FLUOROMETHOLONE; SULFACETAMIDE SODIUM

66 1FLURBIPROFEN SODIUM

67 1FOSCARBIDOPA; FOSLEVODOPA

68 2GATIFLOXACIN

69 1GENTAMICIN SULFATE

70 2GENTAMICIN SULFATE; PREDNISOLONE ACETATE

71 2GLECAPREVIR; PIBRENTASVIR

72 1HEXOCYCLIUM METHYLSULFATE

73 2HYDROCHLOROTHIAZIDE

74 1HYDROCODONE BITARTRATE; IBUPROFEN

75 5HYDROCORTISONE

76 2HYDROXYPROGESTERONE CAPROATE

77 13IBRUTINIB

78 1IDOXURIDINE

79 1IOPAMIDOL

80 1IRON DEXTRAN

81 2ISOPROTERENOL SULFATE

82 4KETOROLAC TROMETHAMINE

83 17LEUPROLIDE ACETATE

84 2LEUPROLIDE ACETATE; NORETHINDRONE ACETATE

85 2LEVOBUNOLOL HYDROCHLORIDE

86 4LEVOMILNACIPRAN HYDROCHLORIDE

87 12LEVOTHYROXINE SODIUM

88 3LINACLOTIDE

89 6LIOTRIX (T4;T3)

90 4LOPINAVIR; RITONAVIR

91 1MEDRYSONE

92 7MEMANTINE HYDROCHLORIDE

93 4MESALAMINE

94 1METHARBITAL

95 2METHYCLOTHIAZIDE

96 4MILNACIPRAN HYDROCHLORIDE

97 1MIRVETUXIMAB SORAVTANSINE-GYNX

98 5MIVACURIUM CHLORIDE

99 12MORPHINE SULFATE

100 1NALBUPHINE HYDROCHLORIDE

101 1NAPHAZOLINE HYDROCHLORIDE

102 4NEBIVOLOL HYDROCHLORIDE

103 1NEBIVOLOL HYDROCHLORIDE; VALSARTAN

104 1NEDOCROMIL SODIUM

105 1NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PREDNISOLONE ACETATE

106 5NIACIN

107 1NITROGLYCERIN

108 1OFLOXACIN

109 1OMBITASVIR; PARITAPREVIR; RITONAVIR

110 3OXYBUTYNIN

111 1OXYBUTYNIN CHLORIDE

112 5OnabotulinumtoxinA

113 5PANCRELIPASE (AMYLASE;LIPASE;PROTEASE)

114 3PARAMETHADIONE

115 6PARICALCITOL

116 1PHENACEMIDE

117 1PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE

118 1PILOCARPINE HYDROCHLORIDE

119 1PODOFILOX

120 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

121 3POTASSIUM CHLORIDE

122 2PREDNISOLONE ACETATE

123 2PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

124 2PROGESTERONE

125 1PROPARACAINE HYDROCHLORIDE

126 1PROTEIN HYDROLYSATE

127 3RISANKIZUMAB-RZAA

128 4RITONAVIR

129 1SELENIUM SULFIDE

130 1SEVOFLURANE

131 2SILODOSIN

132 1SODIUM NITROPRUSSIDE

133 2SUCRALFATE

134 3SULFACETAMIDE SODIUM

135 1SULFADIAZINE

136 1SULFOXONE SODIUM

137 2TELISOTUZUMAB VEDOTIN-TLLV

138 4TESTOSTERONE

139 3TRANDOLAPRIL

140 4TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE

141 2TRETINOIN

142 2TRIAMCINOLONE ACETONIDE

143 3TRIMEPRAZINE TARTRATE

144 3TRIMETHADIONE

145 2TROSPIUM CHLORIDE

146 2UBROGEPANT

147 4UPADACITINIB

148 2URSODIOL

149 1VALPROATE SODIUM

150 2VALPROIC ACID

151 3VENETOCLAX

152 3VILAZODONE HYDROCHLORIDE

filter Dosage Reset all filters

411 All

01 1AEROSOL, METERED;INHALATION

02 2AEROSOL;TOPICAL

03 1CAPSULE, DELAYED REL PELLETS;ORAL

04 8CAPSULE, DELAYED RELEASE;ORAL

05 29CAPSULE, EXTENDED RELEASE;ORAL

06 38CAPSULE;ORAL

07 5CREAM;TOPICAL

08 1CREAM;VAGINAL

09 1EMULSION; OPHTHALMIC

10 2EMULSION;OPHTHALMIC

11 10FILM, EXTENDED RELEASE;TRANSDERMAL

12 5FOR SUSPENSION;ORAL

13 1GEL, METERED;TRANSDERMAL

14 3GEL;TOPICAL

15 1GEL;TRANSDERMAL

16 2GEL;VAGINAL

17 1IMPLANT;INTRAVITREAL

18 1IMPLANT;OPHTHALMIC

19 2INJECTABLE, TABLET;INTRAMUSCULAR, ORAL

20 1INJECTABLE; INJECTION

21 34INJECTABLE;INJECTION

22 1INJECTABLE;INTRA-ARTICULAR, INTRAMUSCULAR, INTRAVITREAL

23 1INJECTABLE;INTRAVENOUS

24 1LIQUID;INHALATION

25 1LOTION/SHAMPOO;TOPICAL

26 1OINTMENT;INTRA-ANAL

27 6OINTMENT;OPHTHALMIC

28 2OINTMENT;TOPICAL

29 1PELLETS;ORAL

30 2POWDER;INHALATION

31 8POWDER;INTRAMUSCULAR

32 5POWDER;INTRAVENOUS

33 1POWDER;ORAL

34 32SOLUTION/DROPS;OPHTHALMIC

35 1SOLUTION/DROPS;TOPICAL

36 1SOLUTION;INTRAMUSCULAR

37 6SOLUTION;INTRAVENOUS

38 8SOLUTION;ORAL

39 3SOLUTION;SUBCUTANEOUS

40 2SOLUTION;TOPICAL

41 2SUPPOSITORY;RECTAL

42 7SUSPENSION/DROPS;OPHTHALMIC

43 1SUSPENSION;ENTERAL

44 1SUSPENSION;INTRATRACHEAL

45 2SUSPENSION;OPHTHALMIC

46 2SUSPENSION;ORAL

47 1SYRINGE

48 2SYRUP;ORAL

49 5TABLET, DELAYED RELEASE;ORAL

50 2TABLET, EXTENDED RELEASE; ORAL

51 21TABLET, EXTENDED RELEASE;ORAL

52 118TABLET;ORAL

53 2TABLET;ORAL-21

54 2TABLET;ORAL-28

55 3TABLET;SUBLINGUAL

56 1VIAL

57 5VIAL; SINGLE-USE

58 2VIAL;SINGLE-DOSE

filter Dosage Strength Reset all filters

411 All

01 10.001MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

02 10.002MG/ML (0.002MG/ML)

03 10.002MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

04 10.005MG/ML (0.005MG/ML)

05 30.01%

06 10.01% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

07 10.0125MG;0.0031MG

08 10.01MG/2ML (0.005MG/ML)

09 30.025%

10 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

11 10.025MG/24HR

12 10.025MG;0.0063MG

13 10.03%

14 20.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

15 20.035MG;0.5MG

16 20.035MG;1MG

17 10.0375%

18 30.05%

19 10.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

20 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

21 10.05MG/24HR

22 10.05MG;0.0125MG

23 10.075%

24 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

25 10.075MG/24HR

26 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

27 50.1%

28 10.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

29 10.1%;10%

30 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

31 10.12%

32 10.12%;0.1%

33 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

34 10.125MG;25MG

35 10.125MG;50MG

36 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

37 10.15%

38 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

39 10.15MG;0.0375MG

40 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

41 10.1MG

42 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

43 10.1MG/24HR

44 10.1MG/INH

45 10.1MG;0.025MG

46 10.2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

47 20.2%;10%

48 10.2%;EQ 0.5% BASE

49 20.25%

50 10.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

51 10.25MG

52 10.25MG;0.0625MG

53 10.25MG;25MG

54 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

55 10.3%

56 10.3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

57 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

58 20.4%

59 10.45%

60 10.4MG/ML

61 10.4MG/ML;100MG/ML

62 10.4MG/ML;50MG/ML

63 10.4MG/ML;75MG/ML

64 80.5%

65 10.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

66 10.7MG

67 61%

68 11%;0.5%

69 11.25%

70 11.5MG/ML

71 310%

72 110% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

73 110,000 UNITS/ML;EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

74 2100 UNITS/VIAL

75 1100%

76 12100MG

77 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

78 1100MG/ML

79 1100MG/PACKET

80 1100MG;25MG

81 1100MG;40MG

82 1100mg/20mL single-dose vial

83 110MCG

84 110MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

85 610MG

86 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

87 110MG/ML

88 110MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

89 110MG;14MG

90 110MG;21MG

91 110MG;28MG

92 110MG;7MG

93 311.25MG

94 111.25MG/VIAL,N/A;N/A,5MG

95 112.5MG

96 112.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

97 1120,000USP UNITS;24,000USP UNITS;76,000USP UNITS

98 1120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

99 1120MG/10ML;2400MG/10ML (12MG/ML;240MG/ML)

100 1125MG

101 1125MG/5ML

102 1125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

103 1125MG/ML

104 113.9%

105 1130MG

106 1133.3MG;33.3MG

107 1134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

108 4140MG

109 1145MCG

110 1145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

111 114MG

112 114MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

113 115,000USP UNITS;3,000USP UNITS;9,500USP UNITS

114 3150MG

115 1150MG/ML

116 215MG

117 1160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

118 1165MG

119 1180,000USP UNITS;36,000USP UNITS;114,000USP UNITS

120 1180MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

121 1187MG/5ML

122 21GM

123 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

124 11GM/10ML

125 11MCG

126 11MG

127 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

128 11MG/ML

129 11MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

130 12% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

131 22.5%

132 12.5MG

133 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

134 12.5MG/24HR

135 1200 UNITS/VIAL

136 2200MG

137 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

138 1200MG/5ML

139 1200MG;50MG

140 120MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

141 320MG

142 220MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

143 120MG/2ML (10MG/ML)

144 121MG

145 122.5MG

146 1230MG

147 1240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

148 125%

149 3250MG

150 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

151 1250MG/5ML

152 2250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

153 1250MG/ML

154 525MG

155 125MG/ML

156 1280MG

157 128MG

158 1290MCG

159 12MCG

160 22MG

161 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

162 12MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

163 12MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

164 12MG;180MG

165 12MG;240MG

166 13%

167 23.75MG

168 13.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

169 13.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

170 13.75MG/VIAL,N/A;N/A,5MG

171 23.9MG/24HR

172 130%

173 130,000USP UNITS;6,000USP UNITS;19,000USP UNITS

174 3300MG

175 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

176 1300MG/ML

177 530MG

178 2325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

179 1325MG;50MG;40MG;30MG

180 1375MG

181 1375MG;500MG;750MG

182 14%

183 14% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

184 14.63MG/ML;20MG/ML

185 1400MG

186 1400MG/VIAL

187 240MG

188 240MG/0.8ML

189 2420MG

190 345MG

191 148MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

192 14MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

193 24MG

194 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

195 14MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

196 14MG;240MG

197 15%

198 250 UNITS/VIAL

199 5500MG

200 4500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

201 1500MG;5MG

202 750MG

203 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

204 150MG;20MG/PACKET

205 154MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

206 2560MG

207 25MG

208 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

209 15MG/24HR

210 15MG/ML

211 160,000USP UNITS;12,000USP UNITS;38,000USP UNITS

212 2600MG/VIAL

213 1600MG;12.5MG

214 1600MG;25MG

215 260MG

216 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

217 161%

218 1660MG;10MG

219 167MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

220 16MG

221 27.5MG

222 17.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

223 17.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

224 370MG

225 170MG/ML

226 172MCG

227 1750MG

228 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

229 1750MG;7.5MG

230 175MG

231 175MG/0.83ML

232 17MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

233 18%

234 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

235 180MG

236 180MG/ML

237 180MG/ML;20MG/ML

238 18MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

239 18MG

240 18MG/0.1ML (8MG/0.1ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

241 1EQ 0.3% BASE

242 1EQ 0.3% BASE;0.6%

243 1EQ 0.3% BASE;1%

244 1EQ 0.35% BASE;10,000 UNITS/ML;0.5%

245 1EQ 0.5GM BASE/VIAL;1.5GM/VIAL

246 1EQ 0.5GM BASE;2GM/VIAL

247 1EQ 0.5MG BASE/ML

248 1EQ 1.5MG BASE

249 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

250 1EQ 100MG IRON/2ML (EQ 50MG IRON/ML)

251 4EQ 10MG BASE

252 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)

253 1EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

254 1EQ 120MG BASE

255 2EQ 125MG VALPROIC ACID

256 1EQ 135MG FENOFIBRIC ACID

257 1EQ 150MG BASE

258 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

259 1EQ 1MG BASE/ML

260 3EQ 2.5MG BASE

261 1EQ 2.5MG BASE/5ML

262 1EQ 200MG BASE

263 1EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

264 4EQ 20MG BASE

265 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML)

266 1EQ 250MG BASE;12.5MG, 75MG, 50MG

267 2EQ 250MG VALPROIC ACID

268 1EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

269 2EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

270 1EQ 2MG SULFATE/0.7ML

271 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

272 1EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE

273 1EQ 3MG BASE

274 1EQ 4.5MG BASE

275 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

276 2EQ 40MG BASE

277 1EQ 45MG FENOFIBRIC ACID

278 1EQ 500MG BASE/VIAL

279 2EQ 500MG VALPROIC ACID

280 1EQ 50MG BASE/100ML

281 1EQ 50MG BASE/ML

282 4EQ 5MG BASE

283 1EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

284 1EQ 5MG BASE;80MG

285 1EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

286 1EQ 60MG BASE

287 1EQ 6MG BASE

288 1EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

289 1EQ 80MG BASE

filter Regulatory Info Reset all filters

411 All

01 235DISCN

02 2OTC

03 143RX

04 31Blank

AbbVie Contract Manufacturing

List of Suppliers

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01

Brand Name : VICODIN HP

BIO Partnering at JPM

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RLD : No

TE Code :

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Dosage Form : TABLET; ORAL

Proprietary Name : VICODIN HP

Dosage Strength : 660MG;10MG

Approval Date : 1996-09-23

Application Number : 40117

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Abbvie Company Banner

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02

Brand Name : VICODIN

BIO Partnering at JPM

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RLD : No

TE Code :

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Dosage Form : TABLET; ORAL

Proprietary Name : VICODIN

Dosage Strength : 500MG;5MG

Approval Date : 1983-01-07

Application Number : 88058

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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03

Brand Name : VICODIN ES

BIO Partnering at JPM

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RLD : No

TE Code :

ACETAMINOPHEN; HYDROCODONE BITARTRATE

Dosage Form : TABLET; ORAL

Proprietary Name : VICODIN ES

Dosage Strength : 750MG;7.5MG

Approval Date : 1988-12-09

Application Number : 89736

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Brand Name : ACYCLOVIR

BIO Partnering at JPM

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RLD : No

TE Code :

ACYCLOVIR SODIUM

Dosage Form : INJECTABLE; INJECTION

Proprietary Name : ACYCLOVIR

Dosage Strength : EQ 50MG BASE/ML

Approval Date : 1999-07-26

Application Number : 75114

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Brand Name : HUMIRA

BIO Partnering at JPM

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RLD :

TE Code :

Dosage Form : SYRINGE

Proprietary Name : HUMIRA

Dosage Strength : 40MG/0.8ML

Approval Date :

Application Number : 125057

RX/OTC/DISCN :

RLD :

TE Code :

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06

Brand Name : HUMIRA

BIO Partnering at JPM

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RLD :

TE Code :

Dosage Form : VIAL

Proprietary Name : HUMIRA

Dosage Strength : 40MG/0.8ML

Approval Date :

Application Number : 125057

RX/OTC/DISCN :

RLD :

TE Code :

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07

Brand Name : LASTACAFT

BIO Partnering at JPM

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RLD : Yes

TE Code :

ALCAFTADINE

Dosage Form : SOLUTION/DROPS; OPHTHALMIC

Proprietary Name : LASTACAFT

Dosage Strength : 0.25%

Approval Date : 2010-07-28

Application Number : 22134

RX/OTC/DISCN : OTC

RLD : Yes

TE Code :

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08

Brand Name : SAPHRIS

BIO Partnering at JPM

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RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Allergan Aesthetics

Dosage Form : TABLET; SUBLINGUAL

Proprietary Name : SAPHRIS

Dosage Strength : EQ 5MG BASE

Approval Date : 2009-08-13

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

Brand Name : SAPHRIS

BIO Partnering at JPM

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RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Allergan Aesthetics

Dosage Form : TABLET; SUBLINGUAL

Proprietary Name : SAPHRIS

Dosage Strength : EQ 10MG BASE

Approval Date : 2009-08-13

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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10

Brand Name : SAPHRIS

BIO Partnering at JPM

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RLD : Yes

TE Code : AB

ASENAPINE MALEATE

Allergan Aesthetics

Dosage Form : TABLET; SUBLINGUAL

Proprietary Name : SAPHRIS

Dosage Strength : EQ 2.5MG BASE

Approval Date : 2015-03-12

Application Number : 22117

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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