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Lansoprazole - 30142-019-14 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 30142-019
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: 30142-019
Labeler Name: The Kroger Co.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202727
Marketing Category: ANDA
Start Marketing Date: 20120901

Package Information of Lansoprazole

Package NDC: 30142-019-14
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (30142-019-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC

NDC Information of Lansoprazole

NDC Code 30142-019-14
Proprietary Name Lansoprazole
Package Description 1 BOTTLE, PLASTIC in 1 BOX (30142-019-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product NDC 30142-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120901
Marketing Category Name ANDA
Labeler Name The Kroger Co.
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lansoprazole


General Information