Nateglinide
- Product NDC
- 68084-458
- 11-digit product format
- 680840458
- Labeler code
- 68084
- Product ID
- 68084-458_ea4005d6-4243-8992-e053-2a95a90a587e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nateglinide
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077463
- Marketing category
- ANDA
- Marketing start
- 2011-01-05
- Marketing end
- 0000-00-00
- Substance
- NATEGLINIDE
- Active strength
- 60 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-458-21 | 68084045821 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-458-21) > 1 TABLET, COATED in 1 BLISTER PACK (68084-458-11) | 30 blister pack | 2011-01-05 | 0000-00-00 | No | No | Current |