Olmesartan Medoxomil
- Product NDC
- 71335-2448
- 11-digit product format
- 713352448
- Labeler code
- 71335
- Product ID
- 71335-2448_75b1de2d-bb52-4457-86f7-80466c0be146
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206763
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- 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 |
|---|
| 71335-2448-1 | 71335244801 | 30 TABLET, COATED in 1 BOTTLE (71335-2448-1) | 2024-08-15 | No | No | Historical |
| 71335-2448-2 | 71335244802 | 60 TABLET, COATED in 1 BOTTLE (71335-2448-2) | 2024-08-15 | No | No | Historical |
| 71335-2448-3 | 71335244803 | 90 TABLET, COATED in 1 BOTTLE (71335-2448-3) | 2024-08-15 | No | No | Historical |
| 71335-2448-4 | 71335244804 | 180 TABLET, COATED in 1 BOTTLE (71335-2448-4) | 2024-08-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Olmesartan Medoxomil | Bryant Ranch Prepack | 2024-08-15 | HUMAN PRESCRIPTION DRUG LABEL | 1 |