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Lansoprazole - 59726-019-42 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 59726-019
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: 59726-019
Labeler Name: P and L Development of New York Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202727
Marketing Category: ANDA
Start Marketing Date: 20130115

Package Information of Lansoprazole

Package NDC: 59726-019-42
Package Description: 3 BOTTLE in 1 BOX (59726-019-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Information of Lansoprazole

NDC Code 59726-019-42
Proprietary Name Lansoprazole
Package Description 3 BOTTLE in 1 BOX (59726-019-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC 59726-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130115
Marketing Category Name ANDA
Labeler Name P and L Development of New York Corporation
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lansoprazole


General Information