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Active Ingredient: MORPHINE SULFATE
Proprietary Name: ASTRAMORPH PF
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.5MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: A071050
Product Number: 001
Approval Date: Oct 7, 1986
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information