ISOSORBIDE MONONITRATE
- Product NDC
- 70518-1080
- 11-digit product format
- 705181080
- Labeler code
- 70518
- Product ID
- 70518-1080_901f1bea-1a01-1ba8-e053-2995a90ae938
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isosorbide mononitrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075395
- Marketing category
- ANDA
- Marketing start
- 2018-03-23
- Marketing end
- 0000-00-00
- Substance
- ISOSORBIDE MONONITRATE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record