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sunmark omeprazole - 49348-846-61 - (Omeprazole)

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Drug Information of sunmark omeprazole

Product NDC: 49348-846
Proprietary Name: sunmark 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 sunmark omeprazole

Product NDC: 49348-846
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080226

Package Information of sunmark omeprazole

Package NDC: 49348-846-61
Package Description: 3 CARTON in 1 CARTON (49348-846-61) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of sunmark omeprazole

NDC Code 49348-846-61
Proprietary Name sunmark omeprazole
Package Description 3 CARTON in 1 CARTON (49348-846-61) > 1 BLISTER PACK in 1 CARTON > 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 49348-846
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080226
Marketing Category Name NDA
Labeler Name McKesson
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of sunmark omeprazole


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