Hydrochlorothiazide
- Product NDC
- 67544-346
- 11-digit product format
- 675440346
- Labeler code
- 67544
- Product ID
- 67544-346_5d3ad7cd-d844-49b9-adde-a05f12d0ea8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040412
- Marketing category
- ANDA
- Marketing start
- 2002-03-29
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 25 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