01 2ANI PHARMS
02 10APOTHECON
03 2BAXTER HLTHCARE
04 6ELKINS SINN
05 3EUGIA PHARMA SPECLTS
06 3FRESENIUS KABI USA
07 12GLAXOSMITHKLINE
08 2HOSPIRA
09 5ISTITUTO BIO ITA SPA
10 2ONESOURCE SPECIALTY
11 3PIRAMAL CRITICAL
12 3SAGENT PHARMS
13 7SANDOZ
14 1TEVA
15 6WATSON LABS INC
16 3WOCKHARDT BIO AG
01 9CAPSULE;ORAL
02 4FOR SOLUTION;ORAL
03 55INJECTABLE;INJECTION
04 2POWDER;INTRAVENOUS
01 57DISCN
02 13RX
01 12BACTOCILL
02 2BACTOCILL IN PLASTIC CONTAINER
03 54OXACILLIN SODIUM
04 2PROSTAPHLIN
01 63No
02 7Yes
RLD : Yes
TE Code :
Brand Name : BACTOCILL IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/ML
Approval Date : 1989-10-26
Application Number : 50640
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : BACTOCILL IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 40MG BASE/ML
Approval Date : 1989-10-26
Application Number : 50640
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : PROSTAPHLIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1982-01-01
Application Number : 50118
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : PROSTAPHLIN
Dosage Form : FOR SOLUTION;ORAL
Dosage Strength : EQ 250MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50194
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : OXACILLIN SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50195
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : OXACILLIN SODIUM
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Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50195
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : OXACILLIN SODIUM
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Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50195
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : OXACILLIN SODIUM
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 : 50195
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : OXACILLIN SODIUM
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 : 50195
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : BACTOCILL
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 : 1982-03-26
Application Number : 61334
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
