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Ondansetron Hydrochloride - 68788-9893-3 - (Ondansetron Hydrochloride)

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Drug Information of Ondansetron Hydrochloride

Product NDC: 68788-9893
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
Coding System: National Drug Codes(NDC)

Labeler Information of Ondansetron Hydrochloride

Product NDC: 68788-9893
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077851
Marketing Category: ANDA
Start Marketing Date: 20120214

Package Information of Ondansetron Hydrochloride

Package NDC: 68788-9893-3
Package Description: 30 TABLET in 1 BOTTLE (68788-9893-3)

NDC Information of Ondansetron Hydrochloride

NDC Code 68788-9893-3
Proprietary Name Ondansetron Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (68788-9893-3)
Product NDC 68788-9893
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ondansetron Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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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