01 6ACETAMINOPHEN
02 1ACETIC ACID, GLACIAL; HYDROCORTISONE
03 1ACYCLOVIR
04 1ALBUTEROL SULFATE
05 2AMIFOSTINE
06 2AMINOPHYLLINE
07 5AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
08 4AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
09 1AMPICILLIN/AMPICILLIN TRIHYDRATE; PROBENECID
10 3BETAMETHASONE DIPROPIONATE
11 1BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
12 3BETAMETHASONE VALERATE
13 1BREMELANOTIDE ACETATE
14 1CAFFEINE; ERGOTAMINE TARTRATE
15 1CALCIPOTRIENE
16 12CAPTOPRIL
17 4CAPTOPRIL; HYDROCHLOROTHIAZIDE
18 1CEVIMELINE HYDROCHLORIDE
19 1CHLORTHALIDONE
20 2CICLOPIROX
21 1CIMETIDINE HYDROCHLORIDE
22 3CITALOPRAM HYDROBROMIDE
23 2CLINDAMYCIN HYDROCHLORIDE
24 3CLOBETASOL PROPIONATE
25 1CLOMIPHENE CITRATE
26 5COLESEVELAM HYDROCHLORIDE
27 1DAPSONE
28 1DESONIDE
29 2DESOXIMETASONE
30 1DIVALPROEX SODIUM
31 3DOXYCYCLINE
32 2ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE
33 2ERYTHROMYCIN ESTOLATE
34 5FLUOCINOLONE ACETONIDE
35 4FLUOCINONIDE
36 2FLUTICASONE PROPIONATE
37 2GENTAMICIN SULFATE
38 1GRISEOFULVIN, MICROSIZE
39 3HALOBETASOL PROPIONATE
40 3HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
41 3HYDROCORTISONE VALERATE
42 1IMIQUIMOD
43 1INDOMETHACIN
44 1KETOCONAZOLE
45 1LIDOCAINE
46 1LIDOCAINE HYDROCHLORIDE
47 1METAPROTERENOL SULFATE
48 4METRONIDAZOLE
49 5MICONAZOLE NITRATE
50 3MOMETASONE FUROATE
51 1NITROGLYCERIN
52 3NYSTATIN
53 2NYSTATIN; TRIAMCINOLONE ACETONIDE
54 3OLMESARTAN MEDOXOMIL
55 6PINDOLOL
56 2PRASUGREL HYDROCHLORIDE
57 1PROCHLORPERAZINE
58 3PROMETHAZINE HYDROCHLORIDE
59 1QUINIDINE SULFATE
60 7ROPINIROLE HYDROCHLORIDE
61 2SELEGILINE HYDROCHLORIDE
62 1SELENIUM SULFIDE
63 1SULFANILAMIDE
64 3TAZAROTENE
65 3TOLAZAMIDE
66 2TOLMETIN SODIUM
67 7TRIAMCINOLONE ACETONIDE
68 2TRIPLE SULFA (SULFABENZAMIDE;SULFACETAMIDE;SULFATHIAZOLE)
01 171COSETTE
01 1BAR, CHEWABLE;ORAL
02 7CAPSULE;ORAL
03 2CREAM, SUPPOSITORY;TOPICAL, VAGINAL
04 24CREAM;TOPICAL
05 4CREAM;VAGINAL
06 3FOR SUSPENSION;ORAL
07 6GEL;TOPICAL
08 1GEL;VAGINAL
09 3INJECTABLE;INJECTION
10 1JELLY;TOPICAL
11 1LOTION/SHAMPOO;TOPICAL
12 5LOTION;TOPICAL
13 1OINTMENT;INTRA-ANAL
14 17OINTMENT;TOPICAL
15 1PASTE;DENTAL
16 1SHAMPOO;TOPICAL
17 1SOLUTION/DROPS;OTIC
18 1SOLUTION;SUBCUTANEOUS
19 5SOLUTION;TOPICAL
20 14SUPPOSITORY;RECTAL
21 2SUPPOSITORY;VAGINAL
22 4SUSPENSION;ORAL
23 1SUSPENSION;TOPICAL
24 2SYRUP;ORAL
25 2TABLET, EXTENDED RELEASE;ORAL
26 61TABLET;ORAL
01 20.005%
02 20.01%
03 50.025%
04 130.05%
05 10.064%;0.005%
06 90.1%
07 30.2%
08 20.25%
09 10.4%
10 10.5%
11 30.75%
12 10.77%
13 11%
14 11.875GM/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 2100,000 UNITS/GM
16 2100,000 UNITS/GM;0.1%
17 1100,000 UNITS/ML
18 6100MG
19 1100MG;2MG
20 310MG
21 110MG/5ML
22 110MG;25MG
23 412.5MG
24 112.5MG;20MG
25 112.5MG;40MG
26 2120MG
27 1125MG/5ML
28 115%
29 32%
30 12%,100MG
31 12%,200MG
32 12%;1%
33 12.5%
34 120MG
35 2250MG
36 525MG
37 125MG;15MG
38 125MG;25MG
39 125MG;40MG
40 23.7%;2.86%;3.42%
41 13.75GM
42 13.75GM/PACKET
43 1300MG
44 130MG
45 2325MG
46 1375MG
47 1375MG/VIAL
48 140MG
49 45%
50 2500MG
51 1500MG/VIAL
52 750MG
53 150MG;15MG
54 150MG;25MG
55 65MG
56 15MG;12.5MG
57 1625MG
58 2650MG
59 18%
60 3EQ 0.05% BASE
61 5EQ 0.1% BASE
62 1EQ 0.25MG BASE
63 1EQ 0.5MG BASE
64 1EQ 1.75MG BASE/0.3ML (EQ 1.75MG BASE/0.3 ML)
65 1EQ 100MG BASE
66 2EQ 10MG BASE
67 1EQ 10MG BASE;12.5MG;40MG
68 1EQ 10MG BASE;20MG
69 1EQ 10MG BASE;25MG;40MG
70 1EQ 10MG BASE;40MG
71 1EQ 125MG BASE/5ML
72 1EQ 150MG BASE
73 1EQ 1MG BASE
74 1EQ 20MG BASE
75 1EQ 250MG BASE/5ML
76 1EQ 2MG BASE
77 1EQ 2MG BASE/5ML
78 1EQ 3.5GM BASE/BOT;1GM/BOT
79 1EQ 300MG BASE
80 1EQ 300MG BASE/2ML
81 1EQ 3MG BASE
82 1EQ 40MG BASE
83 1EQ 4MG BASE
84 1EQ 500MG VALPROIC ACID
85 1EQ 50MG BASE
86 2EQ 5MG BASE
87 1EQ 5MG BASE;12.5MG;20MG
88 1EQ 5MG BASE;12.5MG;40MG
89 1EQ 5MG BASE;20MG
90 1EQ 5MG BASE;25MG;40MG
91 1EQ 5MG BASE;40MG
92 2EQ 600MG BASE
93 1EQ 75MG BASE
01 171USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 120MG
Packaging :
Approval Date : 1982-01-01
Application Number : 18060
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 650MG
Packaging :
Approval Date : 1982-01-01
Application Number : 18060
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 325MG
Packaging :
Approval Date : 1986-12-18
Application Number : 18060
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 120MG
Packaging :
Approval Date : 1992-03-27
Application Number : 72218
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 650MG
Packaging :
Approval Date : 1992-03-27
Application Number : 72237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SUPPOSITORY;RECTAL
Brand Name : ACEPHEN
Dosage Strength : 325MG
Packaging :
Approval Date : 1992-03-27
Application Number : 72344
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ACETIC ACID, GLACIAL; HYDROCORTISONE
Dosage Form : SOLUTION/DROPS;OTIC
Brand Name : HYDROCORTISONE AND ACETIC...
Dosage Strength : 2%;1%
Packaging :
Approval Date : 2006-02-06
Application Number : 40609
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : OINTMENT;TOPICAL
Brand Name : ACYCLOVIR
Dosage Strength : 5%
Packaging :
Approval Date : 2017-11-13
Application Number : 205591
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SYRUP;ORAL
Brand Name : ALBUTEROL SULFATE
Dosage Strength : EQ 2MG BASE/5ML
Packaging :
Approval Date : 1995-09-25
Application Number : 74454
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ETHYOL
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 1995-12-08
Application Number : 20221
Regulatory Info : RX
Registration Country : USA
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