Glyburide

Product NDC: 63739-119
11-digit product format: 637390119
Labeler code: 63739
Product ID: 63739-119_b3c83a08-ebf7-d9cc-e053-2a95a90a3d79
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Glyburide
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA074388
Marketing category: ANDA
Marketing start: 1995-08-30
Marketing end: 2021-07-31
Substance: GLYBURIDE
Active strength: 5 mg/1
Pharmacologic classes: Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
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
63739-119-10	2020-07-22	C162847	48780-1	ab0e2407-35b4-f274-e053-dbdaa90a6471	a56a8f2d-86fc-4deb-a12b-0692c7fd2e5b

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-119-10	EA - Each	63739-119	89f4b3ab-6ee5-415b-a9e0-2f344f57ae7a	1	2012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-119-10	63739011910	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-119-10) > 10 TABLET in 1 BLISTER PACK	10 blister pack	2007-02-27	2021-07-31	No	No	Current