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Ondansetron Hydrochloride - 68084-221-01 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 68084-221
Proprietary Name: Ondansetron Hydrochloride
Non Proprietary Name: Ondansetron Hydrochloride
Active Ingredient(s): 8    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: 68084-221
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078539
Marketing Category: ANDA
Start Marketing Date: 20120501

Package Information of Ondansetron Hydrochloride

Package NDC: 68084-221-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-221-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)

NDC Information of Ondansetron Hydrochloride

NDC Code 68084-221-01
Proprietary Name Ondansetron Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (68084-221-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-221-11)
Product NDC 68084-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120501
Marketing Category Name ANDA
Labeler Name American Health Packaging
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 Hydrochloride


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