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 2CHLORTHALIDONE
07 1EDETATE CALCIUM DISODIUM
08 1ERYTHROMYCIN
09 1FLUDROCORTISONE ACETATE
10 2GLYCOPYRROLATE
11 1HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
12 4MECLIZINE HYDROCHLORIDE
13 2NITROFURANTOIN
14 7NYSTATIN
15 1NYSTATIN; TRIAMCINOLONE ACETONIDE
16 1OXYTETRACYCLINE HYDROCHLORIDE; POLYMYXIN B SULFATE
17 1PENICILLIN G BENZATHINE
18 3PROMETHAZINE HYDROCHLORIDE
19 4TRIAMCINOLONE
20 8TRIAMCINOLONE ACETONIDE
21 1TRIAMCINOLONE DIACETATE
22 1VITAMIN A PALMITATE
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 1SUSPENSION/DROPS;OTIC
11 3SUSPENSION;ORAL
12 1SYRUP;ORAL
13 1TABLET, CHEWABLE, TABLET, CAPSULE;ORAL
14 1TABLET, CHEWABLE;ORAL
15 19TABLET;ORAL
16 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01 20.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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03 30.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 10.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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06 10.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 11%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
08 1100,000 UNITS
09 3100,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 1100,000 UNITS/GM;0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons*
11 1100,000 UNITS/ML
12 1100MG
13 112.5MG
14 112.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 115MG
16 21MG
17 12%
18 1200,000 UNITS
19 1200MG
20 1200MG/ML
21 325MG
22 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 125MG/5ML
24 1262.4MG,N/A,N/A;N/A,250MG,N/A;N/A,N/A,500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 22MG
26 1300MG
27 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**
28 14MG
29 1500,000 UNITS
30 150MG
31 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 150MG/5ML
33 1600,000 UNITS/ML
34 18MG
35 1EQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
36 1EQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM
37 1EQ 4MG BASE/5ML
38 1EQ 50,000 UNITS BASE/ML
39 1EQ 5MG BASE/GM;10,000 UNITS/GM
01 31DISCN
02 17RX
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ZYLOPRIM
Dosage Strength : 100MG
Approval Date : 1982-01-01
Application Number : 16084
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ZYLOPRIM
Dosage Strength : 300MG
Approval Date : 1982-01-01
Application Number : 16084
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ZYLOPRIM
Dosage Strength : 200MG
Approval Date : 2022-08-04
Application Number : 16084
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : IMURAN
Dosage Strength : EQ 100MG BASE/VIAL **Fed...
Approval Date : 1982-01-01
Application Number : 17391
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : OINTMENT; OPHTHALMIC
Proprietary Name : CORTISPORIN
Dosage Strength : 400 UNITS/GM;1%;EQ 3.5MG...
Approval Date : 1982-01-01
Application Number : 50416
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AT
BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : OINTMENT; OPHTHALMIC
Proprietary Name : LUMI-SPORYN
Dosage Strength : EQ 400 UNITS/GM;EQ 3.5MG...
Approval Date : 1982-01-01
Application Number : 50417
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT
RLD : Yes
TE Code :
BISMUTH SUBSALICYLATE; METRONIDAZOLE; TETRACYCLINE HYDROCHLORIDE
Dosage Form : TABLET, CHEWABLE, TABLET, CAPS...
Proprietary Name : HELIDAC
Dosage Strength : 262.4MG,N/A,N/A;N/A,250M...
Approval Date : 1996-08-15
Application Number : 50719
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : THALITONE
Dosage Strength : 15MG
Approval Date : 1988-12-20
Application Number : 19574
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code : BX
Dosage Form : TABLET; ORAL
Proprietary Name : THALITONE
Dosage Strength : 25MG
Approval Date : 1992-02-12
Application Number : 19574
RX/OTC/DISCN : RX
RLD : Yes
TE Code : BX
RLD : No
TE Code :
Dosage Form : INJECTABLE; INJECTION
Proprietary Name : EDETATE CALCIUM DISODIUM
Dosage Strength : 200MG/ML
Approval Date : 2023-05-03
Application Number : 216435
RX/OTC/DISCN : RX
RLD : No
TE Code :
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