Repaglinide
- Product NDC
- 63629-8447
- 11-digit product format
- 636298447
- Labeler code
- 63629
- Product ID
- 63629-8447_09cd2cb6-76d5-4e04-a359-d483e141c674
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- REPAGLINIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201189
- Marketing category
- ANDA
- Marketing start
- 2013-08-09
- Marketing end
- 0000-00-00
- Substance
- REPAGLINIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Glinide [EPC], Potassium Channel Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8447 | REPAGLINIDE TABLET [BRYANT RANCH PREPACK] | 104 | Legacy NDC | 20240511_6768dc76-329a-4ef2-aeae-6814ace18aa0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8447-1 | 63629844701 | 100 TABLET in 1 BOTTLE (63629-8447-1) | 100 tablet | 2013-08-09 | 0000-00-00 | No | No | Current |