OLMESARTAN MEDOXOMIL
- Product NDC
- 71335-2399
- 11-digit product format
- 713352399
- Labeler code
- 71335
- Product ID
- 71335-2399_a638f24b-38b1-4e16-bf18-54d9b99a28d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206720
- Marketing category
- ANDA
- Marketing start
- 2022-03-04
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2399-1 | 71335239901 | 30 TABLET in 1 BOTTLE (71335-2399-1) | 30 tablet | 2024-06-13 | No | No | Historical |
| 71335-2399-2 | 71335239902 | 60 TABLET in 1 BOTTLE (71335-2399-2) | 60 tablet | 2024-06-13 | No | No | Historical |
| 71335-2399-3 | 71335239903 | 90 TABLET in 1 BOTTLE (71335-2399-3) | 90 tablet | 2024-06-13 | No | No | Historical |
| 71335-2399-4 | 71335239904 | 180 TABLET in 1 BOTTLE (71335-2399-4) | 180 tablet | 2024-06-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OLMESARTAN MEDOXOMIL | Bryant Ranch Prepack | 2024-06-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |