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FDA Drug Approval, A213847, DAPSONE
FDA Drug Approval, A213847, DAPSONE
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ANDA: 213847
Company: MYLAN
Drug Name: DAPSONE
Active Ingredients: DAPSONE
Strength: 7.5%
Dosage Form/Route: GEL;TOPICAL
Action Date: 02/04/2022
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: MYLAN
Drug Name: DAPSONE
Active Ingredients: DAPSONE
Strength: 7.5%
Dosage Form/Route: GEL;TOPICAL
Action Date: 02/04/2022
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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