01 3ANI PHARMS
02 1CHARTWELL MOLECULAR
03 1COSETTE
04 1CYCLE
05 1G AND W LABS INC
06 3GLAXOSMITHKLINE
07 11HOSPIRA
08 1LUITPOLD
09 1PAI HOLDINGS PHARM
10 2PH HEALTH
11 2PHARM ASSOC
12 1PHARMOBEDIENT CNSLTG
13 1TEVA PARENTERAL
01 18INJECTABLE;INJECTION
02 11SOLUTION;ORAL
01 27DISCN
02 2RX
01 19CIMETIDINE HYDROCHLORIDE
02 7CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
03 2TAGAMET
04 1TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
01 28No
02 1Yes
RLD : No
TE Code : AA
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 300MG BASE/5ML
Approval Date : 1994-12-22
Application Number : 74251
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 300MG BASE/2ML
Approval Date : 1997-03-28
Application Number : 74296
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 300MG BASE/5ML
Approval Date : 1994-06-01
Application Number : 74176
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : TAGAMET
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 300MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17924
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : TAGAMET
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 300MG BASE/2ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17939
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1985-10-31
Application Number : 19434
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 6MG BASE/ML
Approval Date : 1994-12-27
Application Number : 74269
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 300MG BASE/2ML
Approval Date : 1995-01-31
Application Number : 74344
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 300MG BASE/2ML
Approval Date : 1997-11-26
Application Number : 74252
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CIMETIDINE HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 300MG BASE/2ML
Approval Date : 1994-08-31
Application Number : 74005
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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