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Active Ingredient: OCTREOTIDE ACETATE
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.2MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A077450
Product Number: 001
Approval Date: Feb 10, 2006
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: OCTREOTIDE ACETATE
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A077450
Product Number: 002
Approval Date: Feb 10, 2006
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information