METFORMIN HYDROCHLORIDE

Product NDC
63739-655
11-digit product format
637390655
Labeler code
63739
Product ID
63739-655_eca6f8a3-5b07-4174-9904-6f3105425c45
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA077880
Marketing category
ANDA
Marketing start
2012-12-17
Marketing end
0000-00-00
Substance
METFORMIN HYDROCHLORIDE
Active strength
850 mg/1
Pharmacologic classes
Biguanide [EPC],Biguanides [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-655-102020-07-22C16284748780-1ab0e2407-2f6c-f274-e053-dbdaa90a647160909fe2-ec22-4fa5-ac5c-da143290a378