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Heartburn Relief 24 hour - 70253-019-14 - (Lansoprazole)

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Drug Information of Heartburn Relief 24 hour

Product NDC: 70253-019
Proprietary Name: Heartburn Relief 24 hour
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 Heartburn Relief 24 hour

Product NDC: 70253-019
Labeler Name: OUR FAMILY (Nash Finch Company)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA202727
Marketing Category: ANDA
Start Marketing Date: 20130327

Package Information of Heartburn Relief 24 hour

Package NDC: 70253-019-14
Package Description: 1 BOTTLE in 1 CARTON (70253-019-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

NDC Information of Heartburn Relief 24 hour

NDC Code 70253-019-14
Proprietary Name Heartburn Relief 24 hour
Package Description 1 BOTTLE in 1 CARTON (70253-019-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product NDC 70253-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name ANDA
Labeler Name OUR FAMILY (Nash Finch Company)
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Heartburn Relief 24 hour


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