METFORMIN HYDROCHLORIDE

Product NDC
68645-549
11-digit product format
686450549
Labeler code
68645
Product ID
68645-549_726de4cf-221f-449d-92b1-9f707c9b957f
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
2020-05-31
Substance
METFORMIN HYDROCHLORIDE
Active strength
850 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
68645-549-59EA - Each68645-549447d375d-f131-4500-8eb5-7a1a5556335512017-03-06