Repaglinide
- Product NDC
- 68084-954
- 11-digit product format
- 680840954
- Labeler code
- 68084
- Product ID
- 68084-954_9f0728eb-a746-23bd-e053-2995a90aea9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Repaglinide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077571
- Marketing category
- ANDA
- Marketing start
- 2015-08-24
- Marketing end
- 2020-09-30
- Substance
- REPAGLINIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Glinide [EPC],Potassium Channel Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record