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Octreotide Acetate - 0781-3164-75 - (Octreotide Acetate)

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Drug Information of Octreotide Acetate

Product NDC: 0781-3164
Proprietary Name: Octreotide Acetate
Non Proprietary Name: Octreotide Acetate
Active Ingredient(s): 1000    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: 0781-3164
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019667
Marketing Category: NDA
Start Marketing Date: 19881021

Package Information of Octreotide Acetate

Package NDC: 0781-3164-75
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (0781-3164-75) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Octreotide Acetate

NDC Code 0781-3164-75
Proprietary Name Octreotide Acetate
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (0781-3164-75) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0781-3164
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Octreotide Acetate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19881021
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name OCTREOTIDE ACETATE
Strength Number 1000
Strength Unit ug/mL
Pharmaceutical Classes Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

Complete Information of Octreotide Acetate


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