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FDA Drug Approval, N018961, CHROMIC CHLORIDE IN PLASTIC CONTAINER
FDA Drug Approval, N018961, CHROMIC CHLORIDE IN PLASTIC CONTAINER
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NDA: 018961
Company: HOSPIRA
Drug Name: CHROMIC CHLORIDE IN PLASTIC CONTAINER
Active Ingredients: CHROMIC CHLORIDE
Strength: EQ 0.004MG CHROMIUM/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 06/26/1986
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
Company: HOSPIRA
Drug Name: CHROMIC CHLORIDE IN PLASTIC CONTAINER
Active Ingredients: CHROMIC CHLORIDE
Strength: EQ 0.004MG CHROMIUM/ML
Dosage Form/Route: INJECTABLE;INJECTION
Action Date: 06/26/1986
Marketing Status: Prescription
Submission Classification: Type 5 - New Formulation or New Manufacturer
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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