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Ondansetron - 51079-525-20 - (ondansetron)

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Drug Information of Ondansetron

Product NDC: 51079-525
Proprietary Name: Ondansetron
Non Proprietary Name: ondansetron
Active Ingredient(s): 8    mg/1 & nbsp;   ondansetron
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron

Product NDC: 51079-525
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076930
Marketing Category: ANDA
Start Marketing Date: 20121205

Package Information of Ondansetron

Package NDC: 51079-525-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-525-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-525-01)

NDC Information of Ondansetron

NDC Code 51079-525-20
Proprietary Name Ondansetron
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-525-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-525-01)
Product NDC 51079-525
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of Ondansetron


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