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ondansetron hydrochloride - 55111-154-05 - (ondansetron hydrochloride)

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Drug Information of ondansetron hydrochloride

Product NDC: 55111-154
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: 55111-154
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076183
Marketing Category: ANDA
Start Marketing Date: 20061226

Package Information of ondansetron hydrochloride

Package NDC: 55111-154-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (55111-154-05)

NDC Information of ondansetron hydrochloride

NDC Code 55111-154-05
Proprietary Name ondansetron hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (55111-154-05)
Product NDC 55111-154
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ondansetron hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061226
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
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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