Home > National Drug Code (NDC) > Octreotide acetate

Octreotide acetate - 55648-636-01 - (Octreotide acetate)

Alphabetical Index


Drug Information of Octreotide acetate

Product NDC: 55648-636
Proprietary Name: Octreotide acetate
Non Proprietary Name: Octreotide acetate
Active Ingredient(s): 50    ug/mL & nbsp;   Octreotide acetate
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Octreotide acetate

Product NDC: 55648-636
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090985
Marketing Category: ANDA
Start Marketing Date: 20110511

Package Information of Octreotide acetate

Package NDC: 55648-636-01
Package Description: 1 VIAL in 1 CARTON (55648-636-01) > 1 mL in 1 VIAL

NDC Information of Octreotide acetate

NDC Code 55648-636-01
Proprietary Name Octreotide acetate
Package Description 1 VIAL in 1 CARTON (55648-636-01) > 1 mL in 1 VIAL
Product NDC 55648-636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Octreotide acetate
Dosage Form Name INJECTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20110511
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name OCTREOTIDE ACETATE
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

Complete Information of Octreotide acetate


General Information