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FDA Approval

Tri-Sprintec

CompanyMedVantx, Inc. (DUNS: 806427725)

Effective Date

August 3, 2011

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Manufacturing Establishments (1)

Blenheim Pharmacal, Inc.

Labeler

MedVantx, Inc.

DUNS Number

171434587

Products (1)

Tri-Sprintec

NDC Product Code

66116-436

Application Number

ANDA075808

Marketing Category

ANDA (C73584)

Effective Date

October 29, 2009

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