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AbbVie Inc
FDA Orange Book

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EVENTS

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PRESENTATION(s)

Product List 2025

Product List 2025

DIGITAL CONTENT

1 Corporate Content #SupplierSpotlight, 14 Data Compilation #PharmaFlow, 2786 News #PharmaBuzz

1 Corporate Content #SupplierSpotlight
14 Data Compilation #PharmaFlow
2786 News #PharmaBuzz

ACTIVE PHARMA INGREDIENTS

23 All APIs, 7 USDMF, 6 CEP/COS, 7 KDMF, 5 NDC API, 8 Listed APIs

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

DEVELOPMENTS

1313 Drugs in Development

1313 Drugs in Development

FINISHED DOSAGE FORMULATIONS

1008 FDF Dossiers, 294 FDA Orange Book, 290 Europe, 127 Canada, 233 Australia, 64 South Africa

1008 FDF Dossiers
294 FDA Orange Book
290 Europe
127 Canada
233 Australia
64 South Africa

INSPECTIONS & REGISTRATIONS

94 FDA, 45 EDQM, 2 GDUFA

94 FDA
45 EDQM
2 GDUFA

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filter Active Ingredients Reset all filters

294 All

01 3ACETAMINOPHEN; HYDROCODONE BITARTRATE

02 1ACYCLOVIR SODIUM

03 2ADALIMUMAB

04 1ALCAFTADINE

05 3ATOGEPANT

06 1ATROPINE

07 3ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE

08 1AVIBACTAM SODIUM; AZTREONAM

09 1AVIBACTAM SODIUM; CEFTAZIDIME

10 1BERACTANT

11 4BIMATOPROST

12 1BIPERIDEN HYDROCHLORIDE

13 1BIPERIDEN LACTATE

14 2BRIMONIDINE TARTRATE

15 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE

16 2CALCITRIOL

17 1CARBIDOPA; LEVODOPA

18 4CARIPRAZINE HYDROCHLORIDE

19 3CARTEOLOL HYDROCHLORIDE

20 3CEFDINIR

21 2CEFTAROLINE FOSAMIL

22 2CHOLINE FENOFIBRATE

23 3CISATRACURIUM BESYLATE

24 4CITALOPRAM HYDROBROMIDE

25 8CLARITHROMYCIN

26 6CYCLOSPORINE

27 1DALBAVANCIN HYDROCHLORIDE

28 2DARIFENACIN HYDROBROMIDE

29 1DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR

30 1DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR

31 1DEOXYCHOLIC ACID

32 2DESERPIDINE

33 3DESERPIDINE; HYDROCHLOROTHIAZIDE

34 1DEXAMETHASONE

35 4DEXTROTHYROXINE SODIUM

36 3DICUMAROL

37 2DICYCLOMINE HYDROCHLORIDE

38 8DIVALPROEX SODIUM

39 4DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE

40 1DOXACURIUM CHLORIDE

41 1EFLORNITHINE HYDROCHLORIDE

42 2ELAGOLIX SODIUM

43 1ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM

44 2ELUXADOLINE

45 3EPROSARTAN MESYLATE

46 2EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE

47 4ESCITALOPRAM OXALATE

48 4ESTRADIOL

49 4ETHCHLORVYNOL

50 1FAMOTIDINE

51 8FENOFIBRATE

52 2FLUOROMETHOLONE

53 1FOSCARBIDOPA; FOSLEVODOPA

54 1GATIFLOXACIN

55 2GLECAPREVIR; PIBRENTASVIR

56 1HEXOCYCLIUM METHYLSULFATE

57 2HYDROCHLOROTHIAZIDE

58 1HYDROCODONE BITARTRATE; IBUPROFEN

59 1IOPAMIDOL

60 2ISOPROTERENOL SULFATE

61 3KETOROLAC TROMETHAMINE

62 17LEUPROLIDE ACETATE

63 2LEUPROLIDE ACETATE; NORETHINDRONE ACETATE

64 4LEVOMILNACIPRAN HYDROCHLORIDE

65 12LEVOTHYROXINE SODIUM

66 3LINACLOTIDE

67 4LOPINAVIR; RITONAVIR

68 6MEMANTINE HYDROCHLORIDE

69 4MESALAMINE

70 1METHARBITAL

71 2METHYCLOTHIAZIDE

72 4MILNACIPRAN HYDROCHLORIDE

73 5MIVACURIUM CHLORIDE

74 1NALBUPHINE HYDROCHLORIDE

75 1NEBIVOLOL HYDROCHLORIDE; VALSARTAN

76 5NIACIN

77 1NITROGLYCERIN

78 1OMBITASVIR; PARITAPREVIR; RITONAVIR

79 1OXYBUTYNIN

80 1OXYBUTYNIN CHLORIDE

81 5PANCRELIPASE (AMYLASE;LIPASE;PROTEASE)

82 3PARAMETHADIONE

83 6PARICALCITOL

84 1PHENACEMIDE

85 1PILOCARPINE HYDROCHLORIDE

86 3POTASSIUM CHLORIDE

87 2PREDNISOLONE ACETATE

88 2PROGESTERONE

89 1PROTEIN HYDROLYSATE

90 3RISANKIZUMAB-RZAA

91 4RITONAVIR

92 1SEVOFLURANE

93 2SILODOSIN

94 1SODIUM NITROPRUSSIDE

95 2SUCRALFATE

96 1SULFADIAZINE

97 1SULFOXONE SODIUM

98 2TELISOTUZUMAB VEDOTIN-TLLV

99 4TESTOSTERONE

100 3TRANDOLAPRIL

101 4TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE

102 1TRIAMCINOLONE ACETONIDE

103 3TRIMETHADIONE

104 2UBROGEPANT

105 4UPADACITINIB

106 2URSODIOL

107 1VALPROATE SODIUM

108 2VALPROIC ACID

109 3VENETOCLAX

110 3VILAZODONE HYDROCHLORIDE

filter Dosage Reset all filters

294 All

01 1AEROSOL, METERED;INHALATION

02 1CAPSULE, DELAYED REL PELLETS;ORAL

03 8CAPSULE, DELAYED RELEASE;ORAL

04 12CAPSULE, EXTENDED RELEASE;ORAL

05 31CAPSULE;ORAL

06 1CREAM;TOPICAL

07 2EMULSION;OPHTHALMIC

08 9FILM, EXTENDED RELEASE;TRANSDERMAL

09 5FOR SUSPENSION;ORAL

10 1GEL;TRANSDERMAL

11 2GEL;VAGINAL

12 1IMPLANT;INTRAVITREAL

13 1IMPLANT;OPHTHALMIC

14 2INJECTABLE, TABLET;INTRAMUSCULAR, ORAL

15 1INJECTABLE; INJECTION

16 30INJECTABLE;INJECTION

17 1INJECTABLE;INTRAVENOUS

18 1LIQUID;INHALATION

19 1OINTMENT;INTRA-ANAL

20 1PELLETS;ORAL

21 2POWDER;INHALATION

22 8POWDER;INTRAMUSCULAR

23 5POWDER;INTRAVENOUS

24 1POWDER;ORAL

25 11SOLUTION/DROPS;OPHTHALMIC

26 1SOLUTION/DROPS;TOPICAL

27 1SOLUTION;INTRAMUSCULAR

28 6SOLUTION;INTRAVENOUS

29 7SOLUTION;ORAL

30 3SOLUTION;SUBCUTANEOUS

31 2SUPPOSITORY;RECTAL

32 4SUSPENSION/DROPS;OPHTHALMIC

33 1SUSPENSION;ENTERAL

34 1SUSPENSION;INTRATRACHEAL

35 1SUSPENSION;ORAL

36 1SYRINGE

37 1SYRUP;ORAL

38 5TABLET, DELAYED RELEASE;ORAL

39 2TABLET, EXTENDED RELEASE; ORAL

40 21TABLET, EXTENDED RELEASE;ORAL

41 95TABLET;ORAL

42 1VIAL

43 2VIAL;SINGLE-DOSE

filter Dosage Strength Reset all filters

294 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 10.01%

06 10.01MG/2ML (0.005MG/ML)

07 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

08 10.025MG/24HR

09 10.03%

10 10.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

11 20.05%

12 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

13 10.05MG/24HR

14 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

15 10.075MG/24HR

16 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

17 20.1%

18 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

19 10.12%

20 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

21 10.125MG;25MG

22 10.125MG;50MG

23 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

24 10.15%

25 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

26 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

27 10.1MG

28 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

29 10.1MG/24HR

30 10.1MG/INH

31 10.2%;EQ 0.5% BASE

32 20.25%

33 10.25MG

34 10.25MG;25MG

35 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

36 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium

37 20.4%

38 10.45%

39 10.4MG/ML

40 10.4MG/ML;100MG/ML

41 10.4MG/ML;50MG/ML

42 10.4MG/ML;75MG/ML

43 20.5%

44 10.7MG

45 11%

46 11.25%

47 11.5MG/ML

48 110%

49 110% (100MG/PACKET) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

50 1100%

51 11100MG

52 1100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

53 1100MG/ML

54 1100MG/PACKET

55 1100MG;25MG

56 1100MG;40MG

57 110MCG

58 110MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

59 510MG

60 110MG/ML

61 110MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

62 110MG;14MG

63 110MG;21MG

64 110MG;28MG

65 110MG;7MG

66 311.25MG

67 111.25MG/VIAL,N/A;N/A,5MG

68 112.5MG

69 112.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

70 1120,000USP UNITS;24,000USP UNITS;76,000USP UNITS

71 1120MG/10ML;2400MG/10ML (12MG/ML;240MG/ML)

72 1125MG/5ML

73 1125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

74 113.9%

75 1133.3MG;33.3MG

76 1134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

77 1145MCG

78 1145MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

79 114MG

80 114MG/2.8ML (1MG/0.2ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

81 115,000USP UNITS;3,000USP UNITS;9,500USP UNITS

82 2150MG

83 1150MG/ML

84 215MG

85 1160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

86 1165MG

87 1180,000USP UNITS;36,000USP UNITS;114,000USP UNITS

88 1187MG/5ML

89 21GM

90 11GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

91 11GM/10ML

92 11MCG

93 11MG

94 11MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

95 11MG/ML

96 11MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

97 12.5MG

98 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

99 12.5MG/24HR

100 1200MG

101 1200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

102 1200MG/5ML

103 1200MG;50MG

104 120MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

105 220MG

106 120MG/2ML (10MG/ML)

107 121MG

108 122.5MG

109 125%

110 3250MG

111 2250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

112 1250MG/5ML

113 2250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

114 525MG

115 125MG/ML

116 128MG

117 1290MCG

118 12MCG

119 22MG

120 12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

121 12MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

122 12MG;180MG

123 12MG;240MG

124 23.75MG

125 13.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

126 13.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

127 13.75MG/VIAL,N/A;N/A,5MG

128 13.9MG/24HR

129 130,000USP UNITS;6,000USP UNITS;19,000USP UNITS

130 3300MG

131 1300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

132 1300MG/ML

133 430MG

134 1375MG

135 1375MG;500MG;750MG

136 14%

137 14.63MG/ML;20MG/ML

138 1400MG

139 1400MG/VIAL

140 140MG

141 240MG/0.8ML

142 345MG

143 148MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

144 14MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

145 24MG

146 14MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

147 14MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

148 14MG;240MG

149 15%

150 5500MG

151 4500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

152 1500MG;5MG

153 650MG

154 150MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

155 150MG;20MG/PACKET

156 154MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

157 25MG

158 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

159 15MG/24HR

160 15MG/ML

161 160,000USP UNITS;12,000USP UNITS;38,000USP UNITS

162 2600MG/VIAL

163 1600MG;12.5MG

164 1600MG;25MG

165 160MG

166 161%

167 1660MG;10MG

168 167MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

169 16MG

170 27.5MG

171 17.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

172 17.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

173 172MCG

174 1750MG

175 1750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

176 1750MG;7.5MG

177 175MG

178 175MG/0.83ML

179 17MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

180 18%

181 1800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

182 180MG/ML

183 180MG/ML;20MG/ML

184 18MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

185 18MG

186 1EQ 0.5GM BASE/VIAL;1.5GM/VIAL

187 1EQ 0.5GM BASE;2GM/VIAL

188 1EQ 0.5MG BASE/ML

189 1EQ 1.5MG BASE

190 1EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

191 2EQ 10MG BASE

192 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)

193 1EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

194 1EQ 120MG BASE

195 2EQ 125MG VALPROIC ACID

196 1EQ 135MG FENOFIBRIC ACID

197 1EQ 150MG BASE

198 1EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

199 1EQ 1MG BASE/ML

200 1EQ 200MG BASE

201 1EQ 200MG BASE;8.33MG;50MG;33.33MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

202 3EQ 20MG BASE

203 1EQ 20MG BASE/10ML (EQ 2MG BASE/ML)

204 1EQ 250MG BASE;12.5MG, 75MG, 50MG

205 2EQ 250MG VALPROIC ACID

206 1EQ 2MG BASE/ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

207 2EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

208 1EQ 2MG SULFATE/0.7ML

209 1EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

210 1EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE

211 1EQ 3MG BASE

212 1EQ 4.5MG BASE

213 1EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

214 2EQ 40MG BASE

215 1EQ 45MG FENOFIBRIC ACID

216 1EQ 500MG BASE/VIAL

217 2EQ 500MG VALPROIC ACID

218 1EQ 50MG BASE/100ML

219 1EQ 50MG BASE/ML

220 1EQ 5MG BASE

221 1EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

222 1EQ 5MG BASE;80MG

223 1EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

224 1EQ 60MG BASE

225 1EQ 6MG BASE

226 1EQ 7.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

227 1EQ 80MG BASE

filter Regulatory Info Reset all filters

294 All

01 150DISCN

02 2OTC

03 124RX

04 18Blank

AbbVie Contract Manufacturing

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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

Product
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02

Brand Name : VICODIN

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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 :

Abbvie Company Banner

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03

Brand Name : VICODIN ES

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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

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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

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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 :

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06

Brand Name : HUMIRA

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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 :

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07

Brand Name : LASTACAFT

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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 :

Abbvie Company Banner

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08

Brand Name : QULIPTA

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RLD : Yes

TE Code :

Dosage Form : TABLET; ORAL

Proprietary Name : QULIPTA

Dosage Strength : 10MG

Approval Date : 2021-09-28

Application Number : 215206

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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09

Brand Name : QULIPTA

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RLD : Yes

TE Code :

Dosage Form : TABLET; ORAL

Proprietary Name : QULIPTA

Dosage Strength : 30MG

Approval Date : 2021-09-28

Application Number : 215206

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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10

Brand Name : QULIPTA

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RLD : Yes

TE Code :

Dosage Form : TABLET; ORAL

Proprietary Name : QULIPTA

Dosage Strength : 60MG

Approval Date : 2021-09-28

Application Number : 215206

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

Abbvie Company Banner

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Abbvie Inc is a supplier offers 21 products (APIs, Excipients or Intermediates).

Find a price of Cyclosporine bulk with DMF, CEP offered by Abbvie Inc

Find a price of Erythromycin bulk with DMF, CEP offered by Abbvie Inc

Find a price of Biperiden Hydrochloride bulk with CEP offered by Abbvie Inc

Find a price of Butorphanol Tartrate bulk with DMF offered by Abbvie Inc

Find a price of Erythromycin Ethyl Succinate bulk with DMF offered by Abbvie Inc

Find a price of Erythromycin Stearate bulk with DMF offered by Abbvie Inc

Find a price of Isoflurane bulk with CEP offered by Abbvie Inc

Find a price of Paricalcitol bulk with DMF offered by Abbvie Inc

Find a price of Ritonavir bulk with CEP offered by Abbvie Inc

Find a price of Atogepant bulk offered by Abbvie Inc

Find a price of Divalproex Sodium bulk offered by Abbvie Inc

Find a price of Elagolix Sodium bulk offered by Abbvie Inc

Find a price of Enflurane bulk offered by Abbvie Inc

Find a price of Erythromycin Thiocyanate bulk offered by Abbvie Inc

Find a price of Foscarbidopa bulk offered by Abbvie Inc

Find a price of Foslevodopa bulk offered by Abbvie Inc

Find a price of Glecaprevir bulk offered by Abbvie Inc

Find a price of Levothyroxine Sodium bulk offered by Abbvie Inc

Find a price of Pibrentasvir bulk offered by Abbvie Inc

Find a price of Terazosin HCl bulk offered by Abbvie Inc

Find a price of Venetoclax bulk offered by Abbvie Inc

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