Olmesartan Medoxomil
- Product NDC
- 70518-1345
- 11-digit product format
- 705181345
- Labeler code
- 70518
- Product ID
- 70518-1345_48e9050a-8eab-52eb-e063-6294a90a9d8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA206763
- Marketing category
- ANDA
- Marketing start
- 2018-08-06
- Substance
- OLMESARTAN MEDOXOMIL
- Active strength
- 40 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 | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6M97XTV3HD |
| Rxcui | 349405 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1345-0 | Olmesartan Medoxomil | 90 in 1 BOTTLE, PLASTIC | TABLET, COATED | 90 | | 7 |
| 70518-1345-1 | Olmesartan Medoxomil | 100 in 1 BOTTLE, PLASTIC | TABLET, COATED | 100 | | 7 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-1345-0 | 70518134500 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1345-0) | 2018-08-06 | No | No | Current |
| 70518-1345-1 | 70518134501 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1345-1) | 2025-09-26 | No | No | Current |