HYDROCHLOROTHIAZIDE
- Product NDC
- 50090-7764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA085182
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7764-0 | 30 TABLET in 1 BOTTLE (50090-7764-0) | 2025-11-12 | | No | Historical |
| 50090-7764-2 | 100 TABLET in 1 BOTTLE (50090-7764-2) | 2025-11-12 | | No | Historical |
| 50090-7764-3 | 90 TABLET in 1 BOTTLE (50090-7764-3) | 2025-11-12 | | No | Historical |