Monoket
- Product NDC
- 62175-362
- 11-digit product format
- 621750362
- Labeler code
- 62175
- Product ID
- 62175-362_bd2457f5-22de-4e07-829c-1eadb77e0e9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isosorbide mononitrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- NDA020215
- Marketing category
- NDA
- Marketing start
- 1993-06-30
- Marketing end
- 0000-00-00
- Substance
- ISOSORBIDE MONONITRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62175-362-01 | 62175036201 | 100 TABLET in 1 BOTTLE (62175-362-01) | 100 tablet | 1993-06-30 | 0000-00-00 | No | No | Current |