Hydrochlorothiazide
- Product NDC
- 68788-9401
- 11-digit product format
- 687889401
- Labeler code
- 68788
- Product ID
- 68788-9401_12b0597d-6693-4cd9-8e90-c32056bfef7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040807
- Marketing category
- ANDA
- Marketing start
- 2014-06-16
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 13 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record