isosorbide mononitrate
- Product NDC
- 70518-2206
- 11-digit product format
- 705182206
- Labeler code
- 70518
- Product ID
- 70518-2206_c7028a7f-5884-5476-e053-2995a90aec91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isosorbide mononitrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020215
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-07-11
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2206-0 | 70518220600 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2206-0) | 90 tablet | 2019-07-11 | 0000-00-00 | No | No | Current |