01 1ABC HOLDING
02 2HIKMA
03 2HIKMA INTL PHARMS
04 2LEDERLE
05 4MERCK
06 4NORVIUM BIOSCIENCE
07 2PAR PHARM
08 2RISING
09 1SALIX PHARMS
10 1SANDOZ
11 7WATSON LABS
01 1SUSPENSION;ORAL
02 27TABLET;ORAL
01 27DISCN
02 1RX
01 1ALDOCLOR-150
02 1ALDOCLOR-250
03 13CHLOROTHIAZIDE
04 2CHLOROTHIAZIDE AND RESERPINE
05 2CHLOROTHIAZIDE W/ RESERPINE
06 2CHLOROTHIAZIDE-RESERPINE
07 1DIUPRES-250
08 1DIUPRES-500
09 3DIURIL
10 2METHYLDOPA AND CHLOROTHIAZIDE
01 25No
02 3Yes
RLD : No
TE Code :
Brand Name : CHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1982-09-01
Application Number : 84026
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : DIUPRES-250
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG;0.125MG
Approval Date : 1987-08-26
Application Number : 11635
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : DIUPRES-500
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG;0.125MG
Approval Date : 1987-08-26
Application Number : 11635
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ALDOCLOR-150
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG;250MG
Approval Date : 1982-01-01
Application Number : 16016
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ALDOCLOR-250
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG;250MG
Approval Date : 1982-01-01
Application Number : 16016
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METHYLDOPA AND CHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG;250MG
Approval Date : 1987-11-06
Application Number : 70654
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : METHYLDOPA AND CHLOROTHIAZIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG;250MG
Approval Date : 1987-11-06
Application Number : 70783
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : DIURIL
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 11145
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DIURIL
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 11145
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : DIURIL
Dosage Form : SUSPENSION;ORAL
Dosage Strength : 250MG/5ML
Approval Date : 1982-01-01
Application Number : 11870
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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