01 3ALLOPURINOL
02 1AZATHIOPRINE SODIUM
03 1BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
04 1BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
05 1BISMUTH SUBSALICYLATE; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE
06 4CAMPHOR
07 2CHLORTHALIDONE
08 2DIMENHYDRINATE
09 2DIPHENYLPYRALINE HYDROCHLORIDE
10 1EDETATE CALCIUM DISODIUM
11 1ERYTHROMYCIN
12 2EUCALYPTOL
13 1FLUDROCORTISONE ACETATE
14 2GLYCOPYRROLATE
15 2GUAIACOL
16 4GUAIACOL CARBONATE
17 1HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
18 4MECLIZINE HYDROCHLORIDE
19 2NITROFURANTOIN
20 7NYSTATIN
21 1NYSTATIN; TRIAMCINOLONE ACETONIDE
22 1OXYTETRACYCLINE HYDROCHLORIDE; POLYMYXIN B SULFATE
23 1PENICILLIN G BENZATHINE
24 3PROMETHAZINE HYDROCHLORIDE
25 4TRIAMCINOLONE
26 8TRIAMCINOLONE ACETONIDE
27 1TRIAMCINOLONE DIACETATE
28 1VITAMIN A PALMITATE
01 23CASPER PHARMA LLC
02 24DELCOR ASSET CORP
03 16LABORATOIRES CONFAB INC
04 1RENAISSANCE PHARMA
01 4CREAM;TOPICAL
02 4INJECTABLE;INJECTION
03 4LOTION;TOPICAL
04 3OINTMENT;OPHTHALMIC
05 2OINTMENT;TOPICAL
06 1PASTE;DENTAL
07 1PASTILLE;ORAL
08 1POWDER;TOPICAL
09 1SOLUTION;TOPICAL
10 16SUPPOSITORY
11 1SUSPENSION/DROPS;OTIC
12 3SUSPENSION;ORAL
13 1SYRUP;ORAL
14 1TABLET, CHEWABLE, TABLET, CAPSULE;ORAL
15 1TABLET, CHEWABLE;ORAL
16 19TABLET;ORAL
17 1TABLET;VAGINAL
01 20.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
02 10.1%
03 30.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 10.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 10.5%
06 10.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 10.5MG
08 11%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
09 11.5MG
10 1100,000 UNITS
11 3100,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 1100,000 UNITS/GM;0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
13 1100,000 UNITS/ML
14 3100MG
15 112.5MG
16 112.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 115MG
18 1180MG
19 1185MG
20 21MG
21 12%
22 1200,000 UNITS
23 3200MG
24 1200MG/ML
25 120MG
26 325MG
27 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 125MG/5ML
29 1262.4MG,N/A,N/A;N/A,250MG,N/A;N/A,N/A,500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
30 32MG
31 1300MG
32 1370MG
33 1400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
34 140MG
35 14MG
36 1500,000 UNITS
37 250MG
38 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
39 150MG/5ML
40 15MG
41 1600,000 UNITS/ML
42 1600MG
43 18MG
44 190MG
45 1EQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
46 1EQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM
47 1EQ 4MG BASE/5ML
48 1EQ 50,000 UNITS BASE/ML
49 1EQ 5MG BASE/GM;10,000 UNITS/GM
01 16Canada
02 48USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ZYLOPRIM
Dosage Strength : 100MG
Packaging :
Approval Date : 1982-01-01
Application Number : 16084
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ZYLOPRIM
Dosage Strength : 300MG
Packaging :
Approval Date : 1982-01-01
Application Number : 16084
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ZYLOPRIM
Dosage Strength : 200MG
Packaging :
Approval Date : 2022-08-04
Application Number : 16084
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : IMURAN
Dosage Strength : EQ 100MG BASE/VIAL **F...
Packaging :
Approval Date : 1982-01-01
Application Number : 17391
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : OINTMENT;OPHTHALMIC
Brand Name : CORTISPORIN
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5...
Packaging :
Approval Date : 1982-01-01
Application Number : 50416
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : OINTMENT;OPHTHALMIC
Brand Name : LUMI-SPORYN
Dosage Strength : EQ 400 UNITS/GM;EQ 3.5...
Packaging :
Approval Date : 1982-01-01
Application Number : 50417
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
BISMUTH SUBSALICYLATE; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE
Dosage Form : TABLET, CHEWABLE, TABLET...
Brand Name : HELIDAC
Dosage Strength : 262.4MG,N/A,N/A;N/A,25...
Packaging :
Approval Date : 1996-08-15
Application Number : 50719
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SUPPOSITORY
Brand Name : DEMO-CINEOL ENFANTS/CHILD...
Dosage Strength : 20MG
Packaging : 10
Approval Date :
Application Number : 319724
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SUPPOSITORY
Brand Name : DEMO-CINEOL ADULTES/ADULT...
Dosage Strength : 40MG
Packaging : 10
Approval Date :
Application Number : 319716
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SUPPOSITORY
Brand Name : CREO-RECTAL ADULTES/ADULT...
Dosage Strength : 5MG
Packaging : 10
Approval Date :
Application Number : 299561
Regulatory Info : OTC
Registration Country : Canada
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