isosorbide mononitrate
- Product NDC
- 70934-573
- 11-digit product format
- 709340573
- Labeler code
- 70934
- Product ID
- 70934-573_abfcd0a7-f1c3-83d4-e053-2995a90ae7de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isosorbide mononitrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA075155
- Marketing category
- ANDA
- Marketing start
- 2020-02-26
- 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
- 2021-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-573-30 | 70934057330 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-573-30) | 2020-02-26 | 0000-00-00 | No | No | Current |