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FDA Approval

Zolpidem Tartrate

CompanyAdvanced Rx Pharmacy of Tennessee, LLC (DUNS: 117023142)

Effective Date

November 11, 2022

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Zolpidem(10 mg in 1 1)

Manufacturing Establishments (1)

Advanced Rx Pharmacy of Tennessee, LLC

Labeler

Advanced Rx Pharmacy of Tennessee, LLC

DUNS Number

117023142

Products (1)

Zolpidem Tartrate

NDC Product Code

80425-0060

Application Number

ANDA077322

Marketing Category

ANDA (C73584)

Route of Administration

ORAL

Effective Date

November 11, 2022

Ingredients

Code: WY6W63843KClass: ACTIBQuantity: 10 mg in 1 1

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