Hydrochlorothiazide
- Product NDC
- 50090-6532
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA083177
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6532-0 | 30 TABLET in 1 BOTTLE (50090-6532-0) | 2023-06-22 | | No | Historical |
| 50090-6532-1 | 100 TABLET in 1 BOTTLE (50090-6532-1) | 2023-06-22 | | No | Historical |
| 50090-6532-8 | 90 TABLET in 1 BOTTLE (50090-6532-8) | 2023-06-22 | | No | Historical |