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Approved Drug Products of Abbvie Inc listed in the FDA Orange Book. Original Data : FDA Website

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01 ACETAMINOPHEN; HYDROCODONE BITARTRATE (3)

02 ACYCLOVIR SODIUM (1)

03 ADALIMUMAB (2)

04 ALCAFTADINE (1)

05 ATOGEPANT (3)

06 ATROPINE (1)

07 ATROPINE SULFATE; MEPERIDINE HYDROCHLORIDE (3)

08 BERACTANT (1)

09 BIMATOPROST (4)

10 BIPERIDEN HYDROCHLORIDE (1)

11 BIPERIDEN LACTATE (1)

12 BRIMONIDINE TARTRATE (2)

13 BRIMONIDINE TARTRATE; TIMOLOL MALEATE (1)

14 CALCITRIOL (2)

15 CARBIDOPA; LEVODOPA (1)

16 CARIPRAZINE HYDROCHLORIDE (4)

17 CARTEOLOL HYDROCHLORIDE (3)

18 CEFDINIR (3)

19 CEFTAROLINE FOSAMIL (2)

20 CHOLINE FENOFIBRATE (2)

21 CISATRACURIUM BESYLATE (3)

22 CITALOPRAM HYDROBROMIDE (4)

23 CLARITHROMYCIN (8)

24 CYCLOSPORINE (6)

25 DALBAVANCIN HYDROCHLORIDE (1)

26 DAPSONE (1)

27 DARIFENACIN HYDROBROMIDE (2)

28 DASABUVIR SODIUM; OMBITASVIR, PARITAPREVIR, RITONAVIR (1)

29 DASABUVIR SODIUM; OMBITASVIR; PARITAPREVIR; RITONAVIR (1)

30 DEOXYCHOLIC ACID (1)

31 DESERPIDINE (2)

32 DESERPIDINE; HYDROCHLOROTHIAZIDE (3)

33 DEXAMETHASONE (1)

34 DEXTROTHYROXINE SODIUM (4)

35 DICUMAROL (3)

36 DICYCLOMINE HYDROCHLORIDE (2)

37 DIVALPROEX SODIUM (8)

38 DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE (4)

39 DOXACURIUM CHLORIDE (1)

40 ELAGOLIX SODIUM (2)

41 ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE; ELAGOLIX SODIUM (1)

42 ELUXADOLINE (2)

43 EPROSARTAN MESYLATE (3)

44 EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE (2)

45 ESCITALOPRAM OXALATE (4)

46 ESTRADIOL (4)

47 ETHCHLORVYNOL (4)

48 FAMOTIDINE (1)

49 FENOFIBRATE (8)

50 FLUOROMETHOLONE (2)

51 GATIFLOXACIN (1)

52 GLECAPREVIR; PIBRENTASVIR (2)

53 HEXOCYCLIUM METHYLSULFATE (1)

54 HYDROCHLOROTHIAZIDE (2)

55 HYDROCODONE BITARTRATE; IBUPROFEN (1)

56 IOPAMIDOL (1)

57 ISOPROTERENOL SULFATE (2)

58 KETOROLAC TROMETHAMINE (3)

59 LEUPROLIDE ACETATE (17)

60 LEUPROLIDE ACETATE; NORETHINDRONE ACETATE (2)

61 LEVOMILNACIPRAN HYDROCHLORIDE (4)

62 LEVOTHYROXINE SODIUM (12)

63 LINACLOTIDE (3)

64 LOPINAVIR; RITONAVIR (4)

65 MEMANTINE HYDROCHLORIDE (6)

66 MESALAMINE (4)

67 METHARBITAL (1)

68 METHYCLOTHIAZIDE (2)

69 MILNACIPRAN HYDROCHLORIDE (4)

70 MIVACURIUM CHLORIDE (5)

71 NALBUPHINE HYDROCHLORIDE (1)

72 NEBIVOLOL HYDROCHLORIDE; VALSARTAN (1)

73 NIACIN (5)

74 NITROGLYCERIN (1)

75 OMBITASVIR; PARITAPREVIR; RITONAVIR (1)

76 OXYBUTYNIN (1)

77 OXYBUTYNIN CHLORIDE (1)

78 PANCRELIPASE (AMYLASE;LIPASE;PROTEASE) (5)

79 PARAMETHADIONE (3)

80 PARICALCITOL (6)

81 PHENACEMIDE (1)

82 PILOCARPINE HYDROCHLORIDE (1)

83 POTASSIUM CHLORIDE (3)

84 PREDNISOLONE ACETATE (2)

85 PROTEIN HYDROLYSATE (1)

86 RISANKIZUMAB-RZAA (3)

87 RITONAVIR (4)

88 SEVOFLURANE (1)

89 SODIUM NITROPRUSSIDE (1)

90 SUCRALFATE (2)

91 SULFADIAZINE (1)

92 SULFOXONE SODIUM (1)

93 TESTOSTERONE (4)

94 TRANDOLAPRIL (3)

95 TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE (4)

96 TRIAMCINOLONE ACETONIDE (1)

97 TRIMETHADIONE (3)

98 UBROGEPANT (2)

99 UPADACITINIB (3)

100 VALPROATE SODIUM (1)

101 VALPROIC ACID (2)

102 VENETOCLAX (3)

103 VILAZODONE HYDROCHLORIDE (3)

filter

01 AEROSOL, METERED;INHALATION (1)

02 CAPSULE, DELAYED REL PELLETS;ORAL (1)

03 CAPSULE, DELAYED RELEASE;ORAL (8)

04 CAPSULE, EXTENDED RELEASE;ORAL (12)

05 CAPSULE;ORAL (29)

06 EMULSION;OPHTHALMIC (2)

07 FILM, EXTENDED RELEASE;TRANSDERMAL (9)

08 FOR SUSPENSION;ORAL (5)

09 GEL;TOPICAL (1)

10 GEL;TRANSDERMAL (1)

11 IMPLANT;INTRAVITREAL (1)

12 IMPLANT;OPHTHALMIC (1)

13 INJECTABLE, TABLET;INTRAMUSCULAR, ORAL (2)

14 INJECTABLE; INJECTION (1)

15 INJECTABLE;INJECTION (31)

16 INJECTABLE;INTRAVENOUS (1)

17 LIQUID;INHALATION (1)

18 OINTMENT;INTRA-ANAL (1)

19 PELLETS;ORAL (1)

20 POWDER;INHALATION (2)

21 POWDER;INTRAMUSCULAR (8)

22 POWDER;INTRAVENOUS (3)

23 POWDER;ORAL (1)

24 SOLUTION/DROPS;OPHTHALMIC (10)

25 SOLUTION/DROPS;TOPICAL (1)

26 SOLUTION;INTRAMUSCULAR (1)

27 SOLUTION;INTRAVENOUS (6)

28 SOLUTION;OPHTHALMIC (1)

29 SOLUTION;ORAL (6)

30 SOLUTION;SUBCUTANEOUS (1)

31 SUPPOSITORY;RECTAL (2)

32 SUSPENSION/DROPS;OPHTHALMIC (4)

33 SUSPENSION;ENTERAL (1)

34 SUSPENSION;INTRATRACHEAL (1)

35 SUSPENSION;ORAL (1)

36 SYRINGE (1)

37 SYRUP;ORAL (1)

38 TABLET, DELAYED RELEASE;ORAL (5)

39 TABLET, EXTENDED RELEASE; ORAL (2)

40 TABLET, EXTENDED RELEASE;ORAL (21)

41 TABLET;ORAL (93)

42 VIAL (1)

filter

01 0.001MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

02 0.002MG/ML (0.002MG/ML) (1)

03 0.002MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

04 0.005MG/ML (0.005MG/ML) (1)

05 0.01% (1)

06 0.01MG/2ML (0.005MG/ML) (1)

07 0.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

08 0.025MG/24HR (1)

09 0.03% (1)

10 0.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

11 0.05% (2)

12 0.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

13 0.05MG/24HR (1)

14 0.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

15 0.075MG/24HR (1)

16 0.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

17 0.1% (2)

18 0.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

19 0.12% (1)

20 0.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

21 0.125MG;25MG (1)

22 0.125MG;50MG (1)

23 0.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

24 0.15% (1)

25 0.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

26 0.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

27 0.1MG (1)

28 0.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

29 0.1MG/24HR (1)

30 0.1MG/INH (1)

31 0.2%;EQ 0.5% BASE (1)

32 0.25% (2)

33 0.25MG (1)

34 0.25MG;25MG (1)

35 0.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

36 0.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium (1)

37 0.4% (2)

38 0.45% (1)

39 0.4MG/ML (1)

40 0.4MG/ML;100MG/ML (1)

41 0.4MG/ML;50MG/ML (1)

42 0.4MG/ML;75MG/ML (1)

43 0.5% (2)

44 0.7MG (1)

45 1% (1)

46 1.25% (1)

47 1.5MG/ML (1)

48 10% (1)

49 10% (100MG/PACKET) (1)

50 100% (1)

51 100MG (10)

52 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

53 100MG/ML (1)

54 100MG/PACKET (1)

55 100MG;25MG (1)

56 100MG;40MG (1)

57 10MCG (1)

58 10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

59 10MG (5)

60 10MG/ML (2)

61 10MG;14MG (1)

62 10MG;21MG (1)

63 10MG;28MG (1)

64 10MG;7MG (1)

65 11.25MG (3)

66 11.25MG/VIAL,N/A;N/A,5MG (1)

67 12.5MG (1)

68 12.5MG;75MG;50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

69 120,000USP UNITS;24,000USP UNITS;76,000USP UNITS (1)

70 125MG/5ML (1)

71 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

72 133.3MG;33.3MG (1)

73 134MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

74 145MCG (1)

75 145MG (1)

76 14MG (1)

77 15,000USP UNITS;3,000USP UNITS;9,500USP UNITS (1)

78 150MG (2)

79 150MG/ML (1)

80 15MG (2)

81 160MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

82 165MG (1)

83 180,000USP UNITS;36,000USP UNITS;114,000USP UNITS (1)

84 187MG/5ML (1)

85 1GM (2)

86 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

87 1GM/10ML (1)

88 1MCG (1)

89 1MG (1)

90 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

91 1MG/0.2ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

92 1MG;240MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

93 2.5MG (1)

94 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

95 2.5MG/24HR (1)

96 200MG (1)

97 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

98 200MG/5ML (1)

99 200MG;50MG (1)

100 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

101 20MG (1)

102 20MG/2ML (10MG/ML) (1)

103 21MG (1)

104 22.5MG (1)

105 25% (1)

106 250MG (2)

107 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

108 250MG/5ML (1)

109 250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

110 25MG (5)

111 25MG/ML (1)

112 28MG (1)

113 290MCG (1)

114 2MCG (1)

115 2MG (2)

116 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

117 2MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

118 2MG;180MG (1)

119 2MG;240MG (1)

120 3.75MG (2)

121 3.75MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

122 3.75MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

123 3.75MG/VIAL,N/A;N/A,5MG (1)

124 3.9MG/24HR (1)

125 30,000USP UNITS;6,000USP UNITS;19,000USP UNITS (1)

126 300MG (3)

127 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

128 300MG/ML (1)

129 30MG (4)

130 375MG (1)

131 375MG;500MG;750MG (1)

132 4.63MG/ML;20MG/ML (1)

133 400MG (1)

134 400MG/VIAL (1)

135 40MG (1)

136 40MG/0.8ML (2)

137 45MG (3)

138 48MG (1)

139 4MCG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

140 4MG (1)

141 4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

142 4MG/24HR **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

143 4MG;240MG (1)

144 5% (2)

145 500MG (4)

146 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (4)

147 500MG;5MG (1)

148 50MG (6)

149 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

150 50MG;20MG/PACKET (1)

151 54MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

152 5MG (2)

153 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

154 5MG/24HR (1)

155 5MG/ML (1)

156 60,000USP UNITS;12,000USP UNITS;38,000USP UNITS (1)

157 600MG/VIAL (2)

158 600MG;12.5MG (1)

159 600MG;25MG (1)

160 60MG (1)

161 61% (1)

162 660MG;10MG (1)

163 67MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

164 6MG (1)

165 7.5MG (2)

166 7.5MG,7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

167 7.5MG;200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

168 72MCG (1)

169 750MG (1)

170 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

171 750MG;7.5MG (1)

172 75MG (1)

173 75MG/0.83ML (1)

174 7MG (1)

175 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

176 80MG/ML (1)

177 80MG/ML;20MG/ML (1)

178 8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

179 EQ 0.5MG BASE/ML (1)

180 EQ 1.5MG BASE (1)

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

182 EQ 10MG BASE (2)

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

184 EQ 10MG BASE/ML (1)

185 EQ 120MG BASE (1)

186 EQ 125MG VALPROIC ACID (2)

187 EQ 135MG FENOFIBRIC ACID (1)

188 EQ 150MG BASE (1)

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

190 EQ 1MG BASE/ML (1)

191 EQ 200MG BASE (1)

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

193 EQ 20MG BASE (3)

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

195 EQ 250MG BASE;12.5MG, 75MG, 50MG (1)

196 EQ 250MG VALPROIC ACID (2)

197 EQ 2MG BASE/ML (2)

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

199 EQ 2MG SULFATE/0.7ML (1)

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

201 EQ 300MG BASE,1MG,0.5MG; EQ 300MG BASE (1)

202 EQ 3MG BASE (1)

203 EQ 4.5MG BASE (1)

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

205 EQ 40MG BASE (2)

206 EQ 45MG FENOFIBRIC ACID (1)

207 EQ 500MG BASE/VIAL (1)

208 EQ 500MG VALPROIC ACID (2)

209 EQ 50MG BASE/100ML (1)

210 EQ 50MG BASE/ML (1)

211 EQ 5MG BASE (1)

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

213 EQ 5MG BASE;80MG (1)

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

215 EQ 60MG BASE (1)

216 EQ 6MG BASE (1)

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

218 EQ 80MG BASE (1)

filter

01 DISCN (131)

02 OTC (2)

03 RX (133)

04 Blank (16)

URL Supplier Web Content
TABLET; ORAL
660MG;10MG
1996-09-23
40117
VICODIN HP
DISCN
No
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
500MG;5MG
1983-01-07
88058
VICODIN
DISCN
No
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
750MG;7.5MG
1988-12-09
89736
VICODIN ES
DISCN
No
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
INJECTABLE; INJECT...
EQ 50MG BASE/ML
1999-07-26
75114
ACYCLOVIR
DISCN
No
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
SYRINGE
40MG/0.8ML
125057
HUMIRA
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
VIAL
40MG/0.8ML
125057
HUMIRA
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
SOLUTION/DROPS; OP...
0.25%
2010-07-28
22134
LASTACAFT
OTC
Yes
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
10MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
30MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
URL Supplier Web Content
TABLET; ORAL
60MG
2021-09-28
215206
QULIPTA
RX
Yes
Abbvie Company Banner

Cophex 2024

Not Confirmed

envelop Contact Supplier
Post Enquiry
POST ENQUIRY