REPAGLINIDE
- Product NDC
- 60429-486
- 11-digit product format
- 604290486
- Labeler code
- 60429
- Product ID
- 60429-486_b715903b-1a81-15b5-e053-2a95a90a64bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- REPAGLINIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA091517
- Marketing category
- ANDA
- Marketing start
- 2015-04-24
- Marketing end
- 0000-00-00
- Substance
- REPAGLINIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Glinide [EPC],Potassium Channel Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 60429-486-01 | 60429048601 | 100 TABLET in 1 BOTTLE (60429-486-01) | 100 tablet | 2016-03-26 | 0000-00-00 | No | No | Current |