Glumetza - Metformin hydrochloride 1000 mg / 1 Tablet 90 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

metformin hydrochloride NDC Family 68012-0003 metformin hydrochloride 1000 mg / 1

NDC 11	68012-0003-16
Product NDC	68012-0003
Generic Drug Name	metformin hydrochloride
Brand Name	Glumetza
Manufacturer	Santarus, Inc.
Strength	1000 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	90 Tablet, Film Coated, Extended Release
Package Description	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68012-003-16)
Active Ingredients	Metformin Hydrochloride
Marketing Category	NDA

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NDC snapshot

metformin hydrochloride 1000 mg / 1 Tablet is tracked under NDC 68012-0003-16 and rolls up into product family 68012-0003. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 90 Tablet, Film Coated, Extended Release.
Manufacturer: Santarus, Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familymetformin hydrochloride

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Glumetza - Metformin hydrochloride 1000 mg / 1 Tablet 90 Tablet, Film Coated, Extended Release, NDC 68012-0003-16, is a Santarus, Inc. 1000 mg / 1 tablet presentation packaged as 90 Tablet, Film Coated, Extended Release.

NDC search formats

Canonical NDC 11: 68012-0003-16
Digits-only NDC 11: 68012000316
Possible 10-digit display format: 68012-003-16 (6801200316)

Helpful product links

Search by brand name: Glumetza
Exact NDC 11: 68012-0003-16
Product family NDC: 68012-0003
VA classification code: HS502
VA classification code description: ORAL HYPOGLYCEMIC AGENTS,ORAL
CMOP ID: M1293
VUID: 4041418