Metformin Hydrochloride

Product NDC
68788-7069
11-digit product format
687887069
Labeler code
68788
Product ID
68788-7069_38938c9b-3120-4a04-a619-9ba7c6d17307
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA091184
Marketing category
ANDA
Marketing start
2018-01-03
Marketing end
0000-00-00
Substance
METFORMIN HYDROCHLORIDE
Active strength
500 mg/1
Pharmacologic classes
Biguanide [EPC],Biguanides [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7069-168788706901100 TABLET, FILM COATED in 1 BOTTLE (68788-7069-1) 2018-01-030000-00-00NoNoCurrent
68788-7069-36878870690330 TABLET, FILM COATED in 1 BOTTLE (68788-7069-3) 2018-01-030000-00-00NoNoCurrent
68788-7069-66878870690660 TABLET, FILM COATED in 1 BOTTLE (68788-7069-6) 2018-01-030000-00-00NoNoCurrent
68788-7069-768788706907180 TABLET, FILM COATED in 1 BOTTLE (68788-7069-7) 2018-01-030000-00-00NoNoCurrent
68788-7069-868788706908120 TABLET, FILM COATED in 1 BOTTLE (68788-7069-8) 2018-01-030000-00-00NoNoCurrent
68788-7069-96878870690990 TABLET, FILM COATED in 1 BOTTLE (68788-7069-9) 2018-01-030000-00-00NoNoCurrent