ISOSORBIDE MONONITRATE
- Product NDC
- 68071-3015
- 11-digit product format
- 680713015
- Labeler code
- 68071
- Product ID
- 68071-3015_a4eb5dcb-6b32-4f5d-e053-2a95a90a1cff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ISOSORBIDE MONONITRATE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCarePharmaceuticals, Inc.
- Application
- ANDA200270
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- Marketing end
- 2020-12-31
- Substance
- ISOSORBIDE MONONITRATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record