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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 077331

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NDA 077331 describes OCTREOTIDE ACETATE, which is a drug marketed by Fresenius Kabi Usa, Gland Pharma Ltd, Heritage, Meitheal, Sagent Pharms Inc, Shuangcheng, Sun Pharm Inds, Teva Pharms Usa Inc, West-ward Pharms Int, Wockhardt Usa, and Mylan Institutional, and is included in twenty-two NDAs. It is available from seven suppliers. Additional details are available on the OCTREOTIDE ACETATE profile page.

The generic ingredient in OCTREOTIDE ACETATE is octreotide acetate. There are twenty drug master file entries for this compound. Eleven suppliers are listed for this compound. Additional details are available on the octreotide acetate profile page.

Summary for 077331

Tradename:	OCTREOTIDE ACETATE
Applicant:	Sun Pharm Inds
Ingredient:	octreotide acetate
Patents:	0

Medical Subject Heading (MeSH) Categories for 077331

Antineoplastic Agents, Hormonal
Gastrointestinal Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	INJECTABLE;INJECTION			Strength	EQ 1MG BASE/ML
Approval Date:	Mar 4, 2008	TE:		RLD:	No

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