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kirkland signature omeprazole - 63981-915-55 - (Omeprazole)

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Drug Information of kirkland signature omeprazole

Product NDC: 63981-915
Proprietary Name: kirkland signature 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 kirkland signature omeprazole

Product NDC: 63981-915
Labeler Name: Costco Wholesale Company
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080227

Package Information of kirkland signature omeprazole

Package NDC: 63981-915-55
Package Description: 3 BLISTER PACK in 1 CARTON (63981-915-55) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of kirkland signature omeprazole

NDC Code 63981-915-55
Proprietary Name kirkland signature omeprazole
Package Description 3 BLISTER PACK in 1 CARTON (63981-915-55) > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 63981-915
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080227
Marketing Category Name NDA
Labeler Name Costco Wholesale Company
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of kirkland signature omeprazole


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