Nateglinide
- Product NDC
- 51407-657
- 11-digit product format
- 514070657
- Labeler code
- 51407
- Product ID
- 51407-657_32d5f62e-f2d1-8327-e063-6294a90a91d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- nateglinide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA077463
- Marketing category
- ANDA
- Marketing start
- 2009-09-09
- Substance
- NATEGLINIDE
- Active strength
- 120 mg/1
- Pharmacologic classes
- Glinide [EPC], Potassium Channel Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nateglinide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NATEGLINIDE | 120 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 41X3PWK4O2 |
| Rxcui | 311919, 314142 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-657-01 | Nateglinide | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-657 | NATEGLINIDE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250424_e920b343-f53e-7487-e053-2995a90a719a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-657-01 | 51407065701 | 100 TABLET in 1 BOTTLE, PLASTIC (51407-657-01) | 100 tablet | 2022-05-25 | 0000-00-00 | No | No | Current |