Olmesartan Medoxomil
- Product NDC
- 71335-1074
- 11-digit product format
- 713351074
- Labeler code
- 71335
- Product ID
- 71335-1074_c4b6d748-6473-4408-8e41-8def681662d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Olmesartan Medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204798
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1074-1 | 71335107401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1074-1) | 2019-01-30 | 0000-00-00 | No | No | Current |
| 71335-1074-2 | 71335107402 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1074-2) | 2019-01-30 | 0000-00-00 | No | No | Current |
| 71335-1074-3 | 71335107403 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1074-3) | 2019-01-30 | 0000-00-00 | No | No | Current |
| 71335-1074-4 | 71335107404 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1074-4) | 2019-01-30 | 0000-00-00 | No | No | Current |