Dilatrate
- Product NDC
- 52244-920
- 11-digit product format
- 522440920
- Labeler code
- 52244
- Product ID
- 52244-920_819065d0-0b11-46d4-89f3-578936e32978
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Isosorbide Dinitrate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Endo Pharmaceuticals Inc.
- Application
- NDA019790
- Marketing category
- NDA
- Marketing start
- 2012-02-15
- Marketing end
- 2021-08-31
- Substance
- ISOSORBIDE DINITRATE
- Active strength
- 40 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52244-920-10 | 52244092010 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52244-920-10) | 2012-02-15 | 2021-08-31 | No | No | Current |