Hydrochlorothiazide
- Product NDC
- 60429-215
- 11-digit product format
- 604290215
- Labeler code
- 60429
- Product ID
- 60429-215_7d002ab2-9e17-6500-e053-2a91aa0a6edb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc
- Application
- ANDA203018
- Marketing category
- ANDA
- Marketing start
- 2014-07-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record