01 1ACETAMINOPHEN; CODEINE PHOSPHATE
02 1CORTISONE ACETATE
03 1ERGOCALCIFEROL
04 1FOLIC ACID
05 2HYDROCORTISONE
06 2ISONIAZID
07 1NIACIN
08 1PENTOBARBITAL SODIUM
09 3PREDNISOLONE
10 3PREDNISONE
11 1QUINIDINE SULFATE
12 4RESERPINE
13 1SECOBARBITAL SODIUM
14 1SULFADIAZINE
15 1VITAMIN A
16 2VITAMIN A PALMITATE
01 6CAPSULE;ORAL
02 2CREAM;TOPICAL
03 18TABLET;ORAL
01 10.1MG
02 10.25MG
03 10.5%
04 10.5MG
05 11%
06 3100MG
07 41MG
08 22.5MG
09 1200MG
10 125MG
11 1300MG
12 1325MG;30MG
13 250,000 IU
14 2500MG
15 25MG
16 2EQ 50,000 UNITS BASE
01 26DISCN
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 325MG;30MG
Approval Date : 1982-01-01
Application Number : 85217
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : CORTISONE ACETATE
Dosage Strength : 25MG
Approval Date : 1982-01-01
Application Number : 84246
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : VITAMIN D
Dosage Strength : 50,000 IU
Approval Date : 1982-01-01
Application Number : 80956
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : FOLIC ACID
Dosage Strength : 1MG
Approval Date : 1982-01-01
Application Number : 80755
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : HYDROCORTISONE
Dosage Strength : 0.5%
Approval Date : 1982-01-01
Application Number : 80452
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : HYDROCORTISONE
Dosage Strength : 1%
Approval Date : 1982-01-01
Application Number : 80452
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : STANOZIDE
Dosage Strength : 100MG
Approval Date : 1982-01-01
Application Number : 80126
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : STANOZIDE
Dosage Strength : 300MG
Approval Date : 1982-01-01
Application Number : 80126
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NIACIN
Dosage Strength : 500MG
Approval Date : 1982-01-01
Application Number : 83203
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : SODIUM PENTOBARBITAL
Dosage Strength : 100MG
Approval Date : 1982-01-01
Application Number : 83259
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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