Irbesartan
- Product NDC
- 68084-217
- 11-digit product format
- 680840217
- Labeler code
- 68084
- Product ID
- 68084-217_815466e1-5339-1de9-e053-2991aa0a6991
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Irbesartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA202910
- Marketing category
- ANDA
- Marketing start
- 2014-12-22
- Marketing end
- 2020-06-30
- Substance
- IRBESARTAN
- Active strength
- 150 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record