GLUCOPHAGE - 0087-6064-13 - (METFORMIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of GLUCOPHAGE

Product NDC: 0087-6064
Proprietary Name: GLUCOPHAGE
Non Proprietary Name: METFORMIN HYDROCHLORIDE
Active Ingredient(s): 750    mg/1 & nbsp;   METFORMIN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of GLUCOPHAGE

Product NDC: 0087-6064
Labeler Name: Bristol-Myers Squibb Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021202
Marketing Category: NDA
Start Marketing Date: 20090601

Package Information of GLUCOPHAGE

Package NDC: 0087-6064-13
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0087-6064-13)

NDC Information of GLUCOPHAGE

NDC Code 0087-6064-13
Proprietary Name GLUCOPHAGE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0087-6064-13)
Product NDC 0087-6064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METFORMIN HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name NDA
Labeler Name Bristol-Myers Squibb Company
Substance Name METFORMIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Biguanide [EPC],Biguanides [Chemical/Ingredient]

Complete Information of GLUCOPHAGE


General Information