01 1ACYCLOVIR
02 1ADAPALENE
03 4ALCLOMETASONE DIPROPIONATE
04 7BETAMETHASONE DIPROPIONATE
05 2BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE
06 3BETAMETHASONE VALERATE
07 1CALCIPOTRIENE
08 4CICLOPIROX
09 5CLINDAMYCIN PHOSPHATE
10 10CLOBETASOL PROPIONATE
11 1CLOTRIMAZOLE
12 2DESONIDE
13 2DESOXIMETASONE
14 1DICLOFENAC SODIUM
15 4ERYTHROMYCIN
16 4FLUOCINOLONE ACETONIDE
17 6FLUOCINONIDE
18 5FLUTICASONE PROPIONATE
19 2GENTAMICIN SULFATE
20 2HALOBETASOL PROPIONATE
21 5HYDROCORTISONE
22 1HYDROCORTISONE ACETATE
23 1HYDROCORTISONE VALERATE
24 1IMIQUIMOD
25 1KETOCONAZOLE
26 1LIDOCAINE
27 1LIDOCAINE; PRILOCAINE
28 2METHSCOPOLAMINE BROMIDE
29 3METRONIDAZOLE
30 3MOMETASONE FUROATE
31 1MUPIROCIN
32 2NEOMYCIN SULFATE; TRIAMCINOLONE ACETONIDE
33 1NITROGLYCERIN
34 4NYSTATIN
35 2NYSTATIN; TRIAMCINOLONE ACETONIDE
36 1OXICONAZOLE NITRATE
37 2PREDNICARBATE
38 1SULFACETAMIDE SODIUM
39 2TACROLIMUS
40 1TAZAROTENE
41 3TERCONAZOLE
42 3TETRAHYDROZOLINE HYDROCHLORIDE
43 2TIMOLOL MALEATE
44 8TRIAMCINOLONE ACETONIDE
45 2TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
01 7FOUGERA
02 84FOUGERA PHARMS
03 30FOUGERA PHARMS INC
01 1CREAM, AUGMENTED;TOPICAL
02 39CREAM;TOPICAL
03 4CREAM;VAGINAL
04 1GEL, AUGMENTED;TOPICAL
05 8GEL;TOPICAL
06 1LOTION, AUGMENTED;TOPICAL
07 12LOTION;TOPICAL
08 1OINTMENT, AUGMENTED;TOPICAL
09 30OINTMENT;TOPICAL
10 1OINTMENT;TRANSDERMAL
11 1SHAMPOO;TOPICAL
12 2SOLUTION/DROPS;OPHTHALMIC
13 2SOLUTION;NASAL
14 9SOLUTION;TOPICAL
15 1SPRAY;NASAL
16 1SUPPOSITORY;VAGINAL
17 1SUSPENSION;ORAL
18 1SUSPENSION;TOPICAL
19 1SWAB;TOPICAL
20 2TABLET;ORAL
21 2TABLET;VAGINAL
01 20.005%
02 10.005% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
03 20.01%
04 50.025%
05 10.03%
06 180.05%
07 90.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 140.1%
09 10.2%
10 20.25%
11 10.4%
12 20.5%
13 30.75%
14 30.77%
15 10.8%
16 51%
17 110%
18 1100,000 UNITS
19 2100,000 UNITS/GM
20 2100,000 UNITS/GM;0.1%
21 1100,000 UNITS/ML
22 1184MG;143.75MG;172.5MG
23 72%
24 32.5%
25 12.5%;2.5%
26 12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 13% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 13.7%;2.86%;3.42%
29 35%
30 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
31 180MG
32 7EQ 0.05% BASE
33 2EQ 0.05% BASE;1%
34 5EQ 0.1% BASE
35 1EQ 0.25% BASE
36 1EQ 0.5% BASE
37 5EQ 1% BASE
38 1EQ 2% BASE
39 2EQ 3.5MG BASE/GM;0.1%
01 121USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : ACYCLOVIR
Dosage Strength : 5%
Packaging :
Approval Date : 2016-05-11
Application Number : 206633
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : ADAPALENE
Dosage Strength : 0.1%
Packaging :
Approval Date : 2010-06-30
Application Number : 90824
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : ACLOVATE
Dosage Strength : 0.05% **Federal Regist...
Packaging :
Approval Date : 1982-12-14
Application Number : 18702
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : ACLOVATE
Dosage Strength : 0.05% **Federal Regist...
Packaging :
Approval Date : 1982-12-14
Application Number : 18707
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : ALCLOMETASONE DIPROPIONAT...
Dosage Strength : 0.05%
Packaging :
Approval Date : 2005-07-18
Application Number : 76884
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : ALCLOMETASONE DIPROPIONAT...
Dosage Strength : 0.05%
Packaging :
Approval Date : 2005-07-12
Application Number : 76973
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : BETAMETHASONE DIPROPIONAT...
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1984-09-04
Application Number : 19141
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : BETAMETHASONE DIPROPIONAT...
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 1985-08-12
Application Number : 70275
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : GEL, AUGMENTED;TOPICAL
Brand Name : BETAMETHASONE DIPROPIONAT...
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 2003-05-13
Application Number : 75276
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM, AUGMENTED;TOPICAL
Brand Name : BETAMETHASONE DIPROPIONAT...
Dosage Strength : EQ 0.05% BASE
Packaging :
Approval Date : 2003-12-09
Application Number : 76215
Regulatory Info : RX
Registration Country : USA
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