Nateglinide

Product NDC: 49884-984
11-digit product format: 498840984
Labeler code: 49884
Product ID: 49884-984_20d37769-1721-4531-88cf-e29082373c71
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Nateglinide
Dosage form: TABLET, COATED
Route: ORAL
Labeler: Par Pharmaceutical, Inc.
Application: ANDA077463
Marketing category: ANDA
Marketing start: 2009-09-08
Marketing end: 2024-09-30
Substance: NATEGLINIDE
Active strength: 60 mg/1
Pharmacologic classes: Glinide [EPC], Potassium Channel Antagonists [MoA]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49884-984-01	2022-09-27	C162847	48780-1	e4f33bdf-a80b-d8a0-e053-dadaa90a6e4e	c8ab95a2-82e6-473a-aff3-291306997db6
49884-984-01	2022-07-29	C162847	48780-1	e4f33bdf-a80b-d8a0-e053-dadaa90a6e4e	c8ab95a2-82e6-473a-aff3-291306997db6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49884-984-01	EA - Each	49884-984	ed08dd2f-679a-40f4-a662-244fc2d8e7ee	1	2012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
49884-984-01	49884098401	100 TABLET, COATED in 1 BOTTLE, PLASTIC (49884-984-01)	2009-09-08	2024-09-30	No	No	Current