Chlorothiazide

Product NDC

0378-0162

11-digit product format

003780162

Labeler code

0378

Product ID

0378-0162_4f2271f7-98bc-4b5c-acc6-ad65a717ac84

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

chlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA084217

Marketing category

ANDA

Marketing start

1975-07-17

Marketing end

2020-12-31

Substance

CHLOROTHIAZIDE

Active strength

500 mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record