"0378-0162-01" National Drug Code (NDC)

NDC Code	0378-0162-01
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (0378-0162-01)
Product NDC	0378-0162
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Chlorothiazide
Non-Proprietary Name	Chlorothiazide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19750717
End Marketing Date	20201231
Marketing Category Name	ANDA
Application Number	ANDA084217
Manufacturer	Mylan Pharmaceuticals Inc.
Substance Name	CHLOROTHIAZIDE
Strength	500
Strength Unit	mg/1
Pharmacy Classes	Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]