Olmesartan Medoxomil
- Product NDC
- 71335-0197
- 11-digit product format
- 713350197
- Labeler code
- 71335
- Product ID
- 71335-0197_776aaa8a-f337-4283-b88d-405e34883461
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021286
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-10-26
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0197-1 | 71335019701 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0197-1) | 2017-05-04 | 0000-00-00 | No | No | Current |
| 71335-0197-2 | 71335019702 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0197-2) | 2017-05-04 | 0000-00-00 | No | No | Current |
| 71335-0197-3 | 71335019703 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0197-3) | 2017-05-04 | 0000-00-00 | No | No | Current |