Nateglinide
- Product NDC
- 42291-637
- 11-digit product format
- 422910637
- Labeler code
- 42291
- Product ID
- 42291-637_d57ec136-c9be-ea90-e053-2a95a90a4379
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nateglinide
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA077463
- Marketing category
- ANDA
- Marketing start
- 2016-04-06
- Marketing end
- 0000-00-00
- Substance
- NATEGLINIDE
- Active strength
- 120 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-637-01 | 42291063701 | 100 TABLET, COATED in 1 BOTTLE (42291-637-01) | 2016-04-06 | 0000-00-00 | No | No | Current |