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FDA Drug Approval, N019647, POTASSIUM CITRATE
FDA Drug Approval, N019647, POTASSIUM CITRATE
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NDA: 019647
Company: UT SW MEDCTR
Drug Name: POTASSIUM CITRATE
Active Ingredients: POTASSIUM CITRATE
Strength: 10MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: FOR SOLUTION;ORAL
Action Date: 10/13/1988
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: UT SW MEDCTR
Drug Name: POTASSIUM CITRATE
Active Ingredients: POTASSIUM CITRATE
Strength: 10MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: FOR SOLUTION;ORAL
Action Date: 10/13/1988
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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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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