olmesartan medoxomil
- Product NDC
- 71335-0999
- 11-digit product format
- 713350999
- Labeler code
- 71335
- Product ID
- 71335-0999_5dfd70fb-a8d5-43fa-83fb-ae8723967a3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203281
- Marketing category
- ANDA
- Marketing start
- 2018-08-23
- 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
- 2021-12-31
- 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 |
|---|
| 71335-0999-1 | 71335099901 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0999-1) | 2018-08-23 | 0000-00-00 | No | No | Current |
| 71335-0999-2 | 71335099902 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0999-2) | 2018-08-23 | 0000-00-00 | No | No | Current |
| 71335-0999-3 | 71335099903 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0999-3) | 2018-08-23 | 0000-00-00 | No | No | Current |