HYDROCHLOROTHIAZIDE
- Product NDC
- 50090-7765
- 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
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7765-0 | 90 TABLET in 1 BOTTLE (50090-7765-0) | 2025-11-12 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| HYDROCHLOROTHIAZIDE TABLETS, USP Rx only | A-S Medication Solutions | 2025-11-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |