01 2ANTIBIOTICE
02 4APOTHECON
03 2BAXTER HLTHCARE
04 3EUGIA PHARMA SPECLTS
05 3FRESENIUS
06 6GLAXOSMITHKLINE
07 3ISTITUTO BIO ITA SPA
08 3SAGENT PHARMS
09 6SANDOZ
10 2STERISCIENCE SPECLTS
11 6WATSON LABS INC
12 12WYETH AYERST
01 1CAPSULE;ORAL
02 1FOR SOLUTION;ORAL
03 49INJECTABLE;INJECTION
04 1TABLET;ORAL
01 36DISCN
02 16RX
01 32NAFCILLIN SODIUM
02 6NALLPEN
03 2NALLPEN IN PLASTIC CONTAINER
04 11UNIPEN
05 1UNIPEN IN PLASTIC CONTAINER
01 44No
02 8Yes
RLD : Yes
TE Code :
Brand Name : NALLPEN IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Approval Date : 1989-10-31
Application Number : 50655
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : UNIPEN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 250MG BASE
Approval Date : 1982-01-01
Application Number : 50111
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : UNIPEN
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50199
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : UNIPEN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50320
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : UNIPEN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1982-01-01
Application Number : 50462
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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