Lisinopril and Hydrochlorothiazide
- Product NDC
- 70518-4516
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076230
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70518-4516-0 | 30 TABLET in 1 BLISTER PACK (70518-4516-0) | 2025-11-06 | | No | Historical |
| 70518-4516-1 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4516-1) | 2026-05-13 | | No | Historical |