FDA Drug Approval, A209356, SUCRALFATE
FDA Drug Approval, A209356, SUCRALFATE
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$149.00 USD
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ANDA: 209356
Company: AMNEAL
Drug Name: SUCRALFATE
Active Ingredients: SUCRALFATE
Strength: 1GM/10ML
Dosage Form/Route: SUSPENSION;ORAL
Action Date: 12/02/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: AMNEAL
Drug Name: SUCRALFATE
Active Ingredients: SUCRALFATE
Strength: 1GM/10ML
Dosage Form/Route: SUSPENSION;ORAL
Action Date: 12/02/2019
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB