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up and up lansoprazole - 11673-117-01 - (Lansoprazole)

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Drug Information of up and up lansoprazole

Product NDC: 11673-117
Proprietary Name: up and up lansoprazole
Non Proprietary Name: Lansoprazole
Active Ingredient(s): 15    mg/1 & nbsp;   Lansoprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of up and up lansoprazole

Product NDC: 11673-117
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202319
Marketing Category: ANDA
Start Marketing Date: 20120518

Package Information of up and up lansoprazole

Package NDC: 11673-117-01
Package Description: 1 BOTTLE in 1 CARTON (11673-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Information of up and up lansoprazole

NDC Code 11673-117-01
Proprietary Name up and up lansoprazole
Package Description 1 BOTTLE in 1 CARTON (11673-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC 11673-117
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120518
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up lansoprazole


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