Metformin Hydrochloride

Product NDC
68788-7204
11-digit product format
687887204
Labeler code
68788
Product ID
68788-7204_4d851de2-8ef3-4141-b1f1-aaecd83f3ef7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA078321
Marketing category
ANDA
Marketing start
2018-07-23
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
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7204-168788720401100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7204-1) 2018-07-230000-00-00NoNoCurrent
68788-7204-36878872040330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7204-3) 2018-07-230000-00-00NoNoCurrent
68788-7204-66878872040660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7204-6) 2018-07-230000-00-00NoNoCurrent
68788-7204-868788720408120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7204-8) 2018-07-230000-00-00NoNoCurrent
68788-7204-96878872040990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7204-9) 2018-07-230000-00-00NoNoCurrent