Glipizide

Product NDC: 42708-109
11-digit product format: 427080109
Labeler code: 42708
Product ID: 42708-109_bbb43396-5276-be74-e053-2995a90a5393
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Glipizide
Dosage form: TABLET
Route: ORAL
Labeler: QPharma Inc
Application: ANDA075795
Marketing category: ANDA
Marketing start: 2002-09-25
Marketing end: 0000-00-00
Substance: GLIPIZIDE
Active strength: 5 mg/1
Pharmacologic classes: Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42708-109-30	2021-03-15	C162847	48780-1	ba0f9c33-481e-a910-e053-dadaa90a0b85	GLIPIZIDE TABLETS, USP 5 mg Rx Only
42708-109-30	2021-01-29	C162847	48780-1	ba0f9c33-481e-a910-e053-dadaa90a0b85	GLIPIZIDE TABLETS, USP 5 mg Rx Only

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42708-109	GLIPIZIDE TABLET [QPHARMA INC]	6	Legacy NDC	20241123_3994a267-ddc8-4886-9daa-9adb2ddd0ca3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
42708-109-30	42708010930	30 TABLET in 1 BOTTLE (42708-109-30)	30 tablet	2018-04-26	0000-00-00	Yes	No	Current