Irbesartan
- Product NDC
- 70518-2155
- 11-digit product format
- 705182155
- Labeler code
- 70518
- Product ID
- 70518-2155_8c540b7a-6098-9339-e053-2995a90ad36f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Irbesartan
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202254
- Marketing category
- ANDA
- Marketing start
- 2019-06-27
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record