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FDA Approval

Aurovela Fe 1/20

CompanyAurobindo Pharma Limited (DUNS: 650082092)

Effective Date

November 21, 2023

Labeling Type

Human Prescription Drug Label

Manufacturing Establishments (1)

Aurobindo Pharma Limited

Labeler

Aurobindo Pharma Limited

DUNS Number

650381903

Products (1)

Aurovela Fe 1/20

NDC Product Code

65862-940

Application Number

ANDA207505

Marketing Category

ANDA (C73584)

Effective Date

November 21, 2023

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