olmesartan medoxomil
- Product NDC
- 70771-1059
- 11-digit product format
- 707711059
- Labeler code
- 70771
- Product ID
- 70771-1059_cfde6a89-090d-4b63-a11f-79c4919da819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA205192
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1059-0 | 70771105900 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1059-0) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70771-1059-1 | 70771105901 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1059-1) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70771-1059-3 | 70771105903 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1059-3) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70771-1059-5 | 70771105905 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1059-5) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70771-1059-7 | 70771105907 | 10 BLISTER PACK in 1 CARTON (70771-1059-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1059-2) | 10 blister pack | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70771-1059-9 | 70771105909 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1059-9) | | 2017-04-24 | 0000-00-00 | No | No | Current |