olmesartan medoxomil
- Product NDC
- 70518-2127
- 11-digit product format
- 705182127
- Labeler code
- 70518
- Product ID
- 70518-2127_d6a5bde0-d5ff-8ba8-e053-2a95a90ae06b
- 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
- 2019-06-03
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 70518-2127 | OLMESARTAN MEDOXOMIL TABLET, FILM COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250308_4b6c72a1-3d9a-440e-b047-4ef6370d0122.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2127-0 | 70518212700 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2127-0) | 2019-06-03 | 0000-00-00 | No | No | Current |
| 70518-2127-1 | 70518212701 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2127-1) | 2020-12-14 | 0000-00-00 | No | No | Current |