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Lansoprazole - 21130-019-28 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 21130-019
Proprietary Name: 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 Lansoprazole

Product NDC: 21130-019
Labeler Name: Safeway, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202727
Marketing Category: ANDA
Start Marketing Date: 20121231

Package Information of Lansoprazole

Package NDC: 21130-019-28
Package Description: 2 BOTTLE in 1 BOX (21130-019-28) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Information of Lansoprazole

NDC Code 21130-019-28
Proprietary Name Lansoprazole
Package Description 2 BOTTLE in 1 BOX (21130-019-28) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC 21130-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20121231
Marketing Category Name ANDA
Labeler Name Safeway, Inc.
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lansoprazole


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