Product Details for ANDA 077372
OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
EQ 0.05MG BASE/ML
Marketing Status: Discontinued
EQ 0.1MG BASE/ML
Marketing Status: Discontinued
EQ 0.5MG BASE/ML
Marketing Status: Discontinued
EQ 0.05MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: OCTREOTIDE ACETATE
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.05MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 001
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.05MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 001
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 0.1MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: OCTREOTIDE ACETATE
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.1MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 002
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.1MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 002
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
EQ 0.5MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: OCTREOTIDE ACETATE
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 003
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: OCTREOTIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 0.5MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077372
Product Number: 003
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status: Discontinued
Patent and Exclusivity Information