Nateglinide
- Product NDC
- 0615-7585
- 11-digit product format
- 006157585
- Labeler code
- 0615
- Product ID
- 0615-7585_9edae1d0-63c3-4a88-9902-d07722f1e930
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nateglinide
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077463
- Marketing category
- ANDA
- Marketing start
- 2009-09-08
- Marketing end
- 0000-00-00
- Substance
- NATEGLINIDE
- Active strength
- 60 mg/1
- Pharmacologic classes
- Glinide [EPC],Potassium Channel Antagonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#