Isosorbide Dinitrate
- Product NDC
- 68001-222
- 11-digit product format
- 680010222
- Labeler code
- 68001
- Product ID
- 68001-222_99d54a93-eaf7-5571-e053-2a95a90a477b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isosorbide Dinitrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA089367
- Marketing category
- ANDA
- Marketing start
- 2014-02-06
- Marketing end
- 2021-05-31
- Substance
- ISOSORBIDE DINITRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68001-222-00 | 68001022200 | 100 TABLET in 1 BOTTLE (68001-222-00) | 100 tablet | 2014-02-06 | 2021-05-31 | No | No | Current |
| 68001-222-08 | 68001022208 | 1000 TABLET in 1 BOTTLE (68001-222-08) | 1000 tablet | 2014-02-06 | 2021-05-31 | No | No | Current |