Isosorbide
- Product NDC
- 68071-4390
- 11-digit product format
- 680714390
- Labeler code
- 68071
- Product ID
- 68071-4390_bb7bc6d7-f59d-1a81-e053-2995a90a83bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isosorbide mononitrate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076813
- Marketing category
- ANDA
- Marketing start
- 2006-03-30
- 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
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4390-3 | 68071439003 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4390-3) | 2018-04-11 | 0000-00-00 | No | No | Current |
| 68071-4390-6 | 68071439006 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4390-6) | 2018-04-11 | 0000-00-00 | No | No | Current |
| 68071-4390-9 | 68071439009 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4390-9) | 2018-04-11 | 0000-00-00 | No | No | Current |