Lisinopril and Hydrochlorothiazide
- Product NDC
- 50090-2974
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077912
- Marketing category
- ANDA
- Substance
- HYDROCHLOROTHIAZIDE; LISINOPRIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-2974-0 | 30 TABLET in 1 BOTTLE (50090-2974-0) | 2017-05-18 | | No | Historical |
| 50090-2974-1 | 100 TABLET in 1 BOTTLE (50090-2974-1) | 2017-05-01 | | No | Historical |
| 50090-2974-2 | 90 TABLET in 1 BOTTLE (50090-2974-2) | 2018-08-03 | | No | Historical |