Metformin Hydrochloride

Product NDC
68788-7867
11-digit product format
687887867
Labeler code
68788
Product ID
68788-7867_98dc37e0-fef8-492f-80b8-ced1ad42e235
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA209882
Marketing category
ANDA
Marketing start
2021-02-15
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7867-1EA - Each68788-7867c0ff3b25-cafe-4fe1-ab3d-9882e010690212021-03-02
68788-7867-3EA - Each68788-7867cfd1ffa6-acd1-4d48-813a-040aaabfcc1b12021-03-02
68788-7867-6EA - Each68788-7867d1565536-0836-462c-8441-c7de9eec5a7812021-03-02
68788-7867-7EA - Each68788-786707a6859b-f4b5-46a7-9d12-e82abc8805e412021-03-02
68788-7867-8EA - Each68788-786794142be4-19c9-4cfa-8edd-68100f61ca7a12021-03-02
68788-7867-9EA - Each68788-78674b27f6ff-982d-4e54-85c7-fa9528b8fabf12021-03-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7867-168788786701100 TABLET, FILM COATED in 1 BOTTLE (68788-7867-1) 2021-02-150000-00-00NoNoCurrent
68788-7867-36878878670330 TABLET, FILM COATED in 1 BOTTLE (68788-7867-3) 2021-02-150000-00-00NoNoCurrent
68788-7867-66878878670660 TABLET, FILM COATED in 1 BOTTLE (68788-7867-6) 2021-02-150000-00-00NoNoCurrent
68788-7867-768788786707180 TABLET, FILM COATED in 1 BOTTLE (68788-7867-7) 2021-02-150000-00-00NoNoCurrent
68788-7867-868788786708120 TABLET, FILM COATED in 1 BOTTLE (68788-7867-8) 2021-02-150000-00-00NoNoCurrent
68788-7867-96878878670990 TABLET, FILM COATED in 1 BOTTLE (68788-7867-9) 2021-02-150000-00-00NoNoCurrent