Olmesartan medoxomil
- Product NDC
- 70518-4598
- 11-digit product format
- 705184598
- Labeler code
- 70518
- Product ID
- 70518-4598_4ded3c0e-8510-3590-e063-6294a90a9eb1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan medoxomil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204814
- Marketing category
- ANDA
- Marketing start
- 2026-03-25
- 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
- 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 | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349401 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4598-0 | Olmesartan medoxomil | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4598-0 | 70518459800 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-4598-0) | 100 tablet | 2026-03-25 | No | No | Historical |