Hydrochlorothiazide
- Product NDC
- 0143-1256
- 11-digit product format
- 001431256
- Labeler code
- 0143
- Product ID
- 0143-1256_41215fb1-eeae-491d-99b7-766303842823
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- West-ward Pharmaceutical Corp
- Application
- ANDA084878
- Marketing category
- ANDA
- Marketing start
- 2006-08-01
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
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