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FDA Approval

Aquax-H

CompanyPella Pharmaceuticals Co. ltd (DUNS: 562370925)

Effective Date

December 26, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Hydrocortisone butyrate(30 mg in 30 g)

Products (1)

Aquax-H

NDC Product Code

82160-127

Route of Administration

TOPICAL

Effective Date

December 26, 2023

Ingredients

Hydrocortisone butyrateActive

Code: 05RMF7YPWNClass: ACTIBQuantity: 30 mg in 30 g

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