OLMESARTAN MEDOXOMIL
- Product NDC
- 72303-0848
- 11-digit product format
- 723030848
- Labeler code
- 72303
- Product ID
- 72303-0848_4f4d6ae7-bf66-0418-e063-6394a90afc93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- HEC Pharm USA Inc.
- Application
- ANDA211049
- Marketing category
- ANDA
- Marketing start
- 2026-04-10
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OLMESARTAN MEDOXOMIL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OLMESARTAN MEDOXOMIL | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349373, 349401, 349405 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72303-0848-1 | OLMESARTAN MEDOXOMIL | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 1 |
| 72303-0848-2 | OLMESARTAN MEDOXOMIL | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72303-0848-1 | 72303084801 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72303-0848-1) | 2026-04-10 | No | No | Historical |
| 72303-0848-2 | 72303084802 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72303-0848-2) | 2026-04-10 | No | No | Historical |