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Good Sense Omeprazole - 0113-0915-01 - (Omeprazole)

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Drug Information of Good Sense Omeprazole

Product NDC: 0113-0915
Proprietary Name: Good Sense Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Good Sense Omeprazole

Product NDC: 0113-0915
Labeler Name: L. Perrigo Company
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080228

Package Information of Good Sense Omeprazole

Package NDC: 0113-0915-01
Package Description: 1 BOTTLE in 1 CARTON (0113-0915-01) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE

NDC Information of Good Sense Omeprazole

NDC Code 0113-0915-01
Proprietary Name Good Sense Omeprazole
Package Description 1 BOTTLE in 1 CARTON (0113-0915-01) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Product NDC 0113-0915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080228
Marketing Category Name NDA
Labeler Name L. Perrigo Company
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Good Sense Omeprazole


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