olmesartan medoxomil
- Product NDC
- 42291-542
- 11-digit product format
- 422910542
- Labeler code
- 42291
- Product ID
- 42291-542_d57d3921-085b-6640-e053-2a95a90a6116
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA208130
- Marketing category
- ANDA
- Marketing start
- 2018-09-17
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-542-30 | 42291054230 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-542-30) | 2018-09-17 | 0000-00-00 | No | No | Current |