Benicar
- Product NDC
- 63629-3390
- 11-digit product format
- 636293390
- Labeler code
- 63629
- Product ID
- 63629-3390_aa41c784-2ca3-4c6d-8df2-a38714fbadd8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- olmesartan medoxomil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021286
- Marketing category
- NDA
- Marketing start
- 2002-04-25
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record