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ONDANSETRON - 63304-346-69 - (ONDANSETRON)

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Drug Information of ONDANSETRON

Product NDC: 63304-346
Proprietary Name: ONDANSETRON
Non Proprietary Name: ONDANSETRON
Active Ingredient(s): 4    mg/1 & nbsp;   ONDANSETRON
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of ONDANSETRON

Product NDC: 63304-346
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078602
Marketing Category: ANDA
Start Marketing Date: 20120110

Package Information of ONDANSETRON

Package NDC: 63304-346-69
Package Description: 1 BLISTER PACK in 1 CARTON (63304-346-69) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63304-346-11)

NDC Information of ONDANSETRON

NDC Code 63304-346-69
Proprietary Name ONDANSETRON
Package Description 1 BLISTER PACK in 1 CARTON (63304-346-69) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63304-346-11)
Product NDC 63304-346
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ONDANSETRON
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120110
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name ONDANSETRON
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]

Complete Information of ONDANSETRON


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