Glipizide and Metformin Hydrochloride

Product NDC
0378-3132
11-digit product format
003783132
Labeler code
0378
Product ID
0378-3132_a60e62ce-b960-4bce-a67e-46f913f56247
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
glipizide and metformin hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA078083
Marketing category
ANDA
Marketing start
2007-04-12
Marketing end
2019-11-30
Substance
GLIPIZIDE; METFORMIN HYDROCHLORIDE
Active strength
3 mg/1; mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-3132-01EA - Each0378-31323c4d0e7c-15cf-4615-9e8a-cc594082694212012-07-24