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AcipHex Sprinkle - 62856-241-30 - (rabeprazole sodium)

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Drug Information of AcipHex Sprinkle

Product NDC: 62856-241
Proprietary Name: AcipHex Sprinkle
Non Proprietary Name: rabeprazole sodium
Active Ingredient(s): 10    mg/1 & nbsp;   rabeprazole sodium
Administration Route(s): ORAL
Dosage Form(s): GRANULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of AcipHex Sprinkle

Product NDC: 62856-241
Labeler Name: Eisai Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA204736
Marketing Category: NDA
Start Marketing Date: 20130326

Package Information of AcipHex Sprinkle

Package NDC: 62856-241-30
Package Description: 30 CAPSULE in 1 BOTTLE (62856-241-30) > 1 GRANULE, DELAYED RELEASE in 1 CAPSULE

NDC Information of AcipHex Sprinkle

NDC Code 62856-241-30
Proprietary Name AcipHex Sprinkle
Package Description 30 CAPSULE in 1 BOTTLE (62856-241-30) > 1 GRANULE, DELAYED RELEASE in 1 CAPSULE
Product NDC 62856-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rabeprazole sodium
Dosage Form Name GRANULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130326
Marketing Category Name NDA
Labeler Name Eisai Inc.
Substance Name RABEPRAZOLE SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of AcipHex Sprinkle


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