Glipizide and Metformin Hydrochloride

Product NDC
50090-1550
11-digit product format
500901550
Labeler code
50090
Product ID
50090-1550_5d025c44-8b84-4921-8d95-b4def6e401b8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide and Metformin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077270
Marketing category
ANDA
Marketing start
2005-10-28
Marketing end
0000-00-00
Substance
GLIPIZIDE; METFORMIN HYDROCHLORIDE
Active strength
5 mg/1; mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1550-0EA - Each50090-1550688a565c-b153-4c2b-9d9c-f346e553557712018-11-06