olmesartan medoxomil
- Product NDC
- 70518-2347
- 11-digit product format
- 705182347
- Labeler code
- 70518
- Product ID
- 70518-2347_c85775fe-06b3-1af7-e053-2a95a90a6d7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207662
- Marketing category
- ANDA
- Marketing start
- 2019-10-04
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2347 | OLMESARTAN MEDOXOMIL TABLET, FILM COATED [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250312_c42da0af-84dd-4220-bd40-139be51e8c00.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2347-0 | 70518234700 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2347-0) | 2019-10-04 | 0000-00-00 | No | No | Current |