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FDA Approval

Levonest

CompanyNorthstar Rx LLC (DUNS: 830546433)

Effective Date

November 1, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Registrants (1)

Novast Laboratories, Ltd.

DUNS Number

527695995

Manufacturing Establishments (1)

Novast Laboratories, Ltd.

Labeler

Northstar Rx LLC

Registrant

Novast Laboratories, Ltd.

DUNS Number

527695995

Products (1)

Levonest

NDC Product Code

16714-340

Application Number

ANDA090719

Marketing Category

ANDA (C73584)

Effective Date

November 1, 2023

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