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Up and Up acid reducer - 11673-207-65 - (Famotidine)

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Drug Information of Up and Up acid reducer

Product NDC: 11673-207
Proprietary Name: Up and Up acid reducer
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up acid reducer

Product NDC: 11673-207
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075312
Marketing Category: ANDA
Start Marketing Date: 20090709

Package Information of Up and Up acid reducer

Package NDC: 11673-207-65
Package Description: 3 BLISTER PACK in 1 CARTON (11673-207-65) > 10 TABLET, COATED in 1 BLISTER PACK

NDC Information of Up and Up acid reducer

NDC Code 11673-207-65
Proprietary Name Up and Up acid reducer
Package Description 3 BLISTER PACK in 1 CARTON (11673-207-65) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC 11673-207
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090709
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Up and Up acid reducer


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