olmesartan medoxomil
- Product NDC
- 71335-1920
- 11-digit product format
- 713351920
- Labeler code
- 71335
- Product ID
- 71335-1920_fd68bf4e-5f21-61f7-e053-6294a90a9185
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208130
- Marketing category
- ANDA
- Marketing start
- 2018-06-29
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6M97XTV3HD | OLMESARTAN MEDOXOMIL | 144689-63-4 | OLMESARTAN MEDOXOMIL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-1920-1 | 71335192001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1920-1) | 2021-08-04 | No | No | Historical |
| 71335-1920-2 | 71335192002 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1920-2) | 2021-08-04 | No | No | Historical |
| 71335-1920-3 | 71335192003 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1920-3) | 2021-08-04 | No | No | Historical |
| 71335-1920-4 | 71335192004 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1920-4) | 2021-08-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| olmesartan medoxomil | Bryant Ranch Prepack | 2023-06-05 | HUMAN PRESCRIPTION DRUG LABEL | 101 |