Hydrochlorothiazide
- Product NDC
- 68071-3443
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040707
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-3443-3 | 30 TABLET in 1 BOTTLE (68071-3443-3) | 2023-06-21 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| HYDROCHLOROTHIAZIDE TABLETS, USP | NuCare Pharmaceuticals,Inc. | 2025-04-25 | HUMAN PRESCRIPTION DRUG LABEL | 3 |