METFORMIN HYDROCHLORIDE

Product NDC
68382-039
11-digit product format
683820039
Labeler code
68382
Product ID
68382-039_4ca45053-c36e-40b6-a92a-b773bbbe830d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METFORMIN HYDROCHLORIDE
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Zydus Pharmaceuticals (USA) Inc.
Application
ANDA077078
Marketing category
ANDA
Marketing start
2005-09-28
Marketing end
0000-00-00
Substance
METFORMIN HYDROCHLORIDE
Active strength
750 mg/1
Pharmacologic classes
Biguanide [EPC],Biguanides [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
68382-039-05EA - Each68382-0394004b0cd-62aa-4969-b08b-90853667f87912012-07-24