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lansoprazole - 37808-117-01 - (Lansoprazole)

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Drug Information of lansoprazole

Product NDC: 37808-117
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: 37808-117
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202319
Marketing Category: ANDA
Start Marketing Date: 20120518

Package Information of lansoprazole

Package NDC: 37808-117-01
Package Description: 1 BOTTLE in 1 CARTON (37808-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Information of lansoprazole

NDC Code 37808-117-01
Proprietary Name lansoprazole
Package Description 1 BOTTLE in 1 CARTON (37808-117-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC 37808-117
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 H E B
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of lansoprazole


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