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

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01 ACYCLOVIR (1)

02 ADAPALENE (1)

03 ALCLOMETASONE DIPROPIONATE (4)

04 BETAMETHASONE DIPROPIONATE (7)

05 BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE (2)

06 BETAMETHASONE VALERATE (3)

07 CALCIPOTRIENE (1)

08 CICLOPIROX (4)

09 CLINDAMYCIN PHOSPHATE (5)

10 CLOBETASOL PROPIONATE (10)

11 CLOTRIMAZOLE (1)

12 DESONIDE (2)

13 DESOXIMETASONE (2)

14 DICLOFENAC SODIUM (1)

15 ERYTHROMYCIN (4)

16 FLUOCINOLONE ACETONIDE (4)

17 FLUOCINONIDE (6)

18 FLUTICASONE PROPIONATE (5)

19 GENTAMICIN SULFATE (2)

20 HALOBETASOL PROPIONATE (2)

21 HYDROCORTISONE (5)

22 HYDROCORTISONE ACETATE (1)

23 HYDROCORTISONE VALERATE (1)

24 IMIQUIMOD (1)

25 KETOCONAZOLE (1)

26 LIDOCAINE (1)

27 LIDOCAINE; PRILOCAINE (1)

28 METHSCOPOLAMINE BROMIDE (2)

29 METRONIDAZOLE (3)

30 MOMETASONE FUROATE (3)

31 MUPIROCIN (1)

32 NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE (2)

33 NITROGLYCERIN (1)

34 NYSTATIN (4)

35 NYSTATIN; TRIAMCINOLONE ACETONIDE (2)

36 OXICONAZOLE NITRATE (1)

37 PREDNICARBATE (2)

38 SULFACETAMIDE SODIUM (1)

39 TACROLIMUS (2)

40 TAZAROTENE (1)

41 TERCONAZOLE (3)

42 TETRAHYDROZOLINE HYDROCHLORIDE (3)

43 TIMOLOL MALEATE (2)

44 TRIAMCINOLONE ACETONIDE (8)

45 TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE) (2)

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01 CREAM, AUGMENTED;TOPICAL (1)

02 CREAM;TOPICAL (39)

03 CREAM;VAGINAL (4)

04 GEL, AUGMENTED;TOPICAL (1)

05 GEL;TOPICAL (8)

06 LOTION, AUGMENTED;TOPICAL (1)

07 LOTION;TOPICAL (12)

08 OINTMENT, AUGMENTED;TOPICAL (1)

09 OINTMENT;TOPICAL (30)

10 OINTMENT;TRANSDERMAL (1)

11 SHAMPOO;TOPICAL (1)

12 SOLUTION/DROPS;OPHTHALMIC (2)

13 SOLUTION;NASAL (2)

14 SOLUTION;TOPICAL (9)

15 SPRAY;NASAL (1)

16 SUPPOSITORY;VAGINAL (1)

17 SUSPENSION;ORAL (1)

18 SUSPENSION;TOPICAL (1)

19 SWAB;TOPICAL (1)

20 TABLET;ORAL (2)

21 TABLET;VAGINAL (2)

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01 0.005% (2)

02 0.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

03 0.01% (2)

04 0.025% (5)

05 0.03% (1)

06 0.05% (18)

07 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (9)

08 0.1% (14)

09 0.2% (1)

10 0.25% (2)

11 0.4% (1)

12 0.5% (2)

13 0.75% (3)

14 0.77% (3)

15 0.8% (1)

16 1% (5)

17 10% (1)

18 100,000 UNITS (1)

19 100,000 UNITS/GM (2)

20 100,000 UNITS/GM;0.1% (2)

21 100,000 UNITS/ML (1)

22 184MG;143.75MG;172.5MG (1)

23 2% (7)

24 2.5% (3)

25 2.5%;2.5% (1)

26 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

27 3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

28 3.7%;2.86%;3.42% (1)

29 5% (3)

30 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

31 80MG (1)

32 EQ 0.05% BASE (7)

33 EQ 0.05% BASE;1% (2)

34 EQ 0.1% BASE (5)

35 EQ 0.25% BASE (1)

36 EQ 0.5% BASE (1)

37 EQ 1% BASE (5)

38 EQ 2% BASE (1)

39 EQ 3.5MG BASE/GM;0.1% (2)

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01 DISCN (34)

02 RX (87)

URL Supplier Web Content
OINTMENT; TOPICAL
5%
2016-05-11
206633
ACYCLOVIR
RX
No
AB
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CREAM; TOPICAL
0.1%
2010-06-30
90824
ADAPALENE
RX
No
AB
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OINTMENT; TOPICAL
0.05% **Federal Re...
1982-12-14
18702
ACLOVATE
DISCN
Yes
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CREAM; TOPICAL
0.05% **Federal Re...
1982-12-14
18707
ACLOVATE
DISCN
Yes
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OINTMENT; TOPICAL
0.05%
2005-07-18
76884
ALCLOMETASONE DIPR...
RX
No
AB
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CREAM; TOPICAL
0.05%
2005-07-12
76973
ALCLOMETASONE DIPR...
RX
No
AB
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LOTION; TOPICAL
EQ 0.05% BASE
1985-08-12
70275
BETAMETHASONE DIPR...
RX
No
AB
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OINTMENT, AUGMENTE...
EQ 0.05% BASE
1999-06-22
75373
BETAMETHASONE DIPR...
RX
No
AB
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CREAM, AUGMENTED; ...
EQ 0.05% BASE
2003-12-09
76215
BETAMETHASONE DIPR...
RX
No
AB
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LOTION, AUGMENTED;...
EQ 0.05% BASE
2007-05-21
77111
BETAMETHASONE DIPR...
RX
No
AB
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