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ONDANSETRON HYDROCHLORIDE - 62756-130-02 - (ONDANSETRON HYDROCHLORIDE)

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Drug Information of ONDANSETRON HYDROCHLORIDE

Product NDC: 62756-130
Proprietary Name: ONDANSETRON HYDROCHLORIDE
Non Proprietary Name: ONDANSETRON HYDROCHLORIDE
Active Ingredient(s): 4    mg/1 & nbsp;   ONDANSETRON HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ONDANSETRON HYDROCHLORIDE

Product NDC: 62756-130
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077050
Marketing Category: ANDA
Start Marketing Date: 20070625

Package Information of ONDANSETRON HYDROCHLORIDE

Package NDC: 62756-130-02
Package Description: 10 BLISTER PACK in 1 DOSE PACK (62756-130-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of ONDANSETRON HYDROCHLORIDE

NDC Code 62756-130-02
Proprietary Name ONDANSETRON HYDROCHLORIDE
Package Description 10 BLISTER PACK in 1 DOSE PACK (62756-130-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 62756-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070625
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name ONDANSETRON HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ONDANSETRON HYDROCHLORIDE


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