Glipizide

Product NDC
49999-108
11-digit product format
499990108
Labeler code
49999
Product ID
49999-108_4eda2774-ce9d-44cc-9a89-e200c89efab4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA074305
Marketing category
ANDA
Marketing start
1995-04-07
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-108-30EA - Each49999-108e0eeb6fc-f291-49bf-9663-da73d4efe59b12013-06-04
49999-108-60EA - Each49999-1087076d647-d961-4ed9-93aa-338a28d929f812013-06-04
49999-108-90EA - Each49999-10852ac0dc3-22a5-4bd1-9f35-83805620c07712013-09-04