OLMESARTAN MEDOXOMIL
- Product NDC
- 71335-2569
- 11-digit product format
- 713352569
- Labeler code
- 71335
- Product ID
- 71335-2569_0f5b17f1-7d06-48f2-88cd-46e4d36d6f83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208659
- Marketing category
- ANDA
- Marketing start
- 2024-03-30
- Marketing end
- 2026-06-30
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- 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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2569-1 | 71335256901 | 90 TABLET, COATED in 1 BOTTLE (71335-2569-1) | 2025-02-05 | 2026-06-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| OLMESARTAN MEDOXOMIL | Bryant Ranch Prepack | 2025-02-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |