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Octreotide Acetate - 0703-3333-01 - (Octreotide Acetate)

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Drug Information of Octreotide Acetate

Product NDC: 0703-3333
Proprietary Name: Octreotide Acetate
Non Proprietary Name: Octreotide Acetate
Active Ingredient(s): 200    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: 0703-3333
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075959
Marketing Category: ANDA
Start Marketing Date: 20051123

Package Information of Octreotide Acetate

Package NDC: 0703-3333-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3333-01) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Octreotide Acetate

NDC Code 0703-3333-01
Proprietary Name Octreotide Acetate
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3333-01) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0703-3333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Octreotide Acetate
Dosage Form Name INJECTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20051123
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name OCTREOTIDE ACETATE
Strength Number 200
Strength Unit ug/mL
Pharmaceutical Classes Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

Complete Information of Octreotide Acetate


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