isosorbide mononitrate
- Product NDC
- 70518-0009
- 11-digit product format
- 705180009
- Labeler code
- 70518
- Product ID
- 70518-0009_814f68f1-4cf7-6ddb-e053-2991aa0a2aec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isosorbide mononitrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075155
- Marketing category
- ANDA
- Marketing start
- 2016-11-21
- 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