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FDA Drug Approval, A211644, TRETINOIN
FDA Drug Approval, A211644, TRETINOIN
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ANDA: 211644
Company: TARO
Drug Name: TRETINOIN
Active Ingredients: TRETINOIN
Strength: 0.05%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 01/25/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB1
Company: TARO
Drug Name: TRETINOIN
Active Ingredients: TRETINOIN
Strength: 0.05%
Dosage Form/Route: CREAM;TOPICAL
Action Date: 01/25/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB1
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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