Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 077373

Expand all

OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
EQ 0.2MG BASE/ML
Marketing Status: Discontinued

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: 
Application Number: A077373
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)
EQ 1MG BASE/ML
Marketing Status: Discontinued

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: 
Application Number: A077373
Product Number: 002
Approval Date: Aug 14, 2007
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information