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Ondansetron - 0641-6078-25 - (Ondansetron)

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Drug Information of Ondansetron

Product NDC: 0641-6078
Proprietary Name: Ondansetron
Non Proprietary Name: Ondansetron
Active Ingredient(s): 2    mg/mL & nbsp;   Ondansetron
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 0641-6078
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077541
Marketing Category: ANDA
Start Marketing Date: 20061226

Package Information of Ondansetron

Package NDC: 0641-6078-25
Package Description: 25 VIAL in 1 CARTON (0641-6078-25) > 2 mL in 1 VIAL (0641-6078-01)

NDC Information of Ondansetron

NDC Code 0641-6078-25
Proprietary Name Ondansetron
Package Description 25 VIAL in 1 CARTON (0641-6078-25) > 2 mL in 1 VIAL (0641-6078-01)
Product NDC 0641-6078
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20061226
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp.
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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