01 3ACS DOBFAR
02 4ACS DOBFAR SPA
03 6ANTIBIOTICE
04 5APOTHECON
05 3ASTRAL
06 5BRISTOL
07 5CONSOLIDATED PHARM
08 11EUGIA PHARMA SPECLTS
09 8GLAXOSMITHKLINE
10 1HANFORD GC
11 9HIKMA
12 5HOSPIRA
13 5HOSPIRA INC
14 12HQ SPECLT PHARMA
15 2INTL MEDICATION
16 9ISTITUTO BIO ITA SPA
17 3LILLY
18 2MEDIMETRIKS PHARMS
19 6PFIZER
20 6SAGENT PHARMS INC
21 13SANDOZ
22 8STERISCIENCE SPECLTS
23 6WATSON LABS INC
24 16WYETH AYERST
01 151INJECTABLE;INJECTION
02 2POWDER;INTRAVENOUS
01 87DISCN
02 65RX
03 1Blank
01 37AMPICILLIN AND SULBACTAM
02 81AMPICILLIN SODIUM
03 10OMNIPEN-N
04 6PENBRITIN-S
05 5POLYCILLIN-N
06 8TOTACILLIN-N
07 6UNASYN
01 143No
02 9Yes
03 1Blank
RLD : No
TE Code :
Brand Name : POLYCILLIN-N
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : POLYCILLIN-N
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Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : POLYCILLIN-N
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Dosage Strength : EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : POLYCILLIN-N
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Dosage Strength : EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50309
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
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Dosage Strength : EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
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 : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
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 : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
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 : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : PENBRITIN-S
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 : 50072
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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