Chlorothiazide
- Product NDC
- 0378-0150
- 11-digit product format
- 003780150
- Labeler code
- 0378
- Product ID
- 0378-0150_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
- 1975-06-26
- Marketing end
- 2020-12-31
- Substance
- CHLOROTHIAZIDE
- Active strength
- 250 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