FDA Drug Approval, A070755, LITHIUM CITRATE
FDA Drug Approval, A070755, LITHIUM CITRATE
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$149.00 USD
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ANDA: 070755
Company: PAI HOLDINGS PHARM
Drug Name: LITHIUM CITRATE
Active Ingredients: LITHIUM CITRATE
Strength: EQ 300MG CARBONATE/5ML
Dosage Form/Route: SYRUP;ORAL
Action Date: 05/21/1986
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None
Company: PAI HOLDINGS PHARM
Drug Name: LITHIUM CITRATE
Active Ingredients: LITHIUM CITRATE
Strength: EQ 300MG CARBONATE/5ML
Dosage Form/Route: SYRUP;ORAL
Action Date: 05/21/1986
Marketing Status: Discontinued
Submission Classification: ORIG-1 TE Code: None