olmesartan medoxomil
- Product NDC
- 70518-2212
- 11-digit product format
- 705182212
- Labeler code
- 70518
- Product ID
- 70518-2212_97383347-eb71-b486-e053-2a95a90a07d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207662
- Marketing category
- ANDA
- Marketing start
- 2019-07-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record