Hydrochlorothiazide
- Product NDC
- 68788-9919
- 11-digit product format
- 687889919
- Labeler code
- 68788
- Product ID
- 68788-9919_f46deca7-c260-4767-812a-84086bddf8a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2012-01-30
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record