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Granisetron - 66758-035-01 - (Granisetron)

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Drug Information of Granisetron

Product NDC: 66758-035
Proprietary Name: Granisetron
Non Proprietary Name: Granisetron
Active Ingredient(s): 1    mg/mL & nbsp;   Granisetron
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Granisetron

Product NDC: 66758-035
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078835
Marketing Category: ANDA
Start Marketing Date: 20080630

Package Information of Granisetron

Package NDC: 66758-035-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (66758-035-01) > 1 mL in 1 VIAL, SINGLE-USE

NDC Information of Granisetron

NDC Code 66758-035-01
Proprietary Name Granisetron
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (66758-035-01) > 1 mL in 1 VIAL, SINGLE-USE
Product NDC 66758-035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20080630
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name GRANISETRON HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Granisetron


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