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FDA Drug Approval, N019670, CLARITIN-D
FDA Drug Approval, N019670, CLARITIN-D
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NDA: 019670
Company: BAYER HEALTHCARE LLC
Drug Name: CLARITIN-D
Active Ingredients: LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength: 5MG;120MG
Dosage Form/Route: TABLET, EXTENDED RELEASE;ORAL
Action Date: 11/14/1994
Marketing Status: Over-the-counter
Submission Classification: Type 4 - New Combination
Company: BAYER HEALTHCARE LLC
Drug Name: CLARITIN-D
Active Ingredients: LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength: 5MG;120MG
Dosage Form/Route: TABLET, EXTENDED RELEASE;ORAL
Action Date: 11/14/1994
Marketing Status: Over-the-counter
Submission Classification: Type 4 - New Combination
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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