ISOSORBIDE MONONITRATE
- Product NDC
- 50090-0786
- 11-digit product format
- 500900786
- Labeler code
- 50090
- Product ID
- 50090-0786_5a520310-462a-4620-9af9-7302e36dfa1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ISOSORBIDE MONONITRATE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200270
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| LX1OH63030 | ISOSORBIDE MONONITRATE | 16051-77-7 | ISOSORBIDE MONONITRATE |