Home > National Drug Code (NDC) > Octreotide Acetate

Octreotide Acetate - 62756-351-44 - (Octreotide Acetate)

Alphabetical Index


Drug Information of Octreotide Acetate

Product NDC: 62756-351
Proprietary Name: Octreotide Acetate
Non Proprietary Name: Octreotide Acetate
Active Ingredient(s): 500    ug/mL & nbsp;   Octreotide Acetate
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Octreotide Acetate

Product NDC: 62756-351
Labeler Name: SUN PHARMACEUTICAL INDUSTRIES LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077372
Marketing Category: ANDA
Start Marketing Date: 20070814

Package Information of Octreotide Acetate

Package NDC: 62756-351-44
Package Description: 10 AMPULE in 1 PACKAGE (62756-351-44) > 1 mL in 1 AMPULE

NDC Information of Octreotide Acetate

NDC Code 62756-351-44
Proprietary Name Octreotide Acetate
Package Description 10 AMPULE in 1 PACKAGE (62756-351-44) > 1 mL in 1 AMPULE
Product NDC 62756-351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Octreotide Acetate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20070814
Marketing Category Name ANDA
Labeler Name SUN PHARMACEUTICAL INDUSTRIES LIMITED
Substance Name OCTREOTIDE ACETATE
Strength Number 500
Strength Unit ug/mL
Pharmaceutical Classes Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

Complete Information of Octreotide Acetate


General Information