Metformin Hydrochloride

Product NDC
42708-039
11-digit product format
427080039
Labeler code
42708
Product ID
42708-039_e07341db-1fb6-40ea-9850-272240ad424a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
QPharma Inc
Application
ANDA077095
Marketing category
ANDA
Marketing start
2005-01-14
Marketing end
0000-00-00
Substance
METFORMIN HYDROCHLORIDE
Active strength
1000 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
42708-039-302021-03-12C16284748780-1ba0f9c33-3459-a910-e053-dadaa90a0b856d452920-71a3-426a-8cf5-3b69e97a9a45
42708-039-302021-01-29C16284748780-1ba0f9c33-3459-a910-e053-dadaa90a0b856d452920-71a3-426a-8cf5-3b69e97a9a45