METFORMIN HYDROCHLORIDE

Product NDC
68645-539
11-digit product format
686450539
Labeler code
68645
Product ID
68645-539_b5703a75-f525-6737-e053-2995a90a0b1c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METFORMIN HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Legacy Pharmaceutical Packaging, LLC
Application
ANDA203686
Marketing category
ANDA
Marketing start
2014-12-09
Marketing end
2021-01-31
Substance
METFORMIN HYDROCHLORIDE
Active strength
500 mg/1
Pharmacologic classes
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
68645-539-59EA - Each68645-539b00659ed-54ec-4dcf-b3f0-12df5654972f12017-03-06