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Granisetron Hydrochloride - 0143-9744-01 - (Granisetron Hydrochloride)

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Drug Information of Granisetron Hydrochloride

Product NDC: 0143-9744
Proprietary Name: Granisetron Hydrochloride
Non Proprietary Name: Granisetron Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Granisetron Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Granisetron Hydrochloride

Product NDC: 0143-9744
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078629
Marketing Category: ANDA
Start Marketing Date: 20091223

Package Information of Granisetron Hydrochloride

Package NDC: 0143-9744-01
Package Description: 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01)

NDC Information of Granisetron Hydrochloride

NDC Code 0143-9744-01
Proprietary Name Granisetron Hydrochloride
Package Description 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01)
Product NDC 0143-9744
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Granisetron Hydrochloride
Dosage Form Name SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091223
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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 Hydrochloride


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