olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- Product NDC
- 72162-1516
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206137
- Marketing category
- ANDA
- Substance
- AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-1516-9 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-1516-9) | 2016-10-26 | | No | Historical |