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equaline omeprazole - 41163-915-74 - (Omeprazole)

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Drug Information of equaline omeprazole

Product NDC: 41163-915
Proprietary Name: equaline 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 equaline omeprazole

Product NDC: 41163-915
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080222

Package Information of equaline omeprazole

Package NDC: 41163-915-74
Package Description: 1 BLISTER PACK in 1 CARTON (41163-915-74) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of equaline omeprazole

NDC Code 41163-915-74
Proprietary Name equaline omeprazole
Package Description 1 BLISTER PACK in 1 CARTON (41163-915-74) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 41163-915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080222
Marketing Category Name NDA
Labeler Name Supervalu Inc
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of equaline omeprazole


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