OMESEC - 16853-1308-3 - (Omeprazole)

Alphabetical Index


Drug Information of OMESEC

Product NDC: 16853-1308
Proprietary Name: OMESEC
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of OMESEC

Product NDC: 16853-1308
Labeler Name: Corporacion Infarmasa
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075410
Marketing Category: ANDA
Start Marketing Date: 20100228

Package Information of OMESEC

Package NDC: 16853-1308-3
Package Description: 42 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (16853-1308-3)

NDC Information of OMESEC

NDC Code 16853-1308-3
Proprietary Name OMESEC
Package Description 42 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (16853-1308-3)
Product NDC 16853-1308
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100228
Marketing Category Name ANDA
Labeler Name Corporacion Infarmasa
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of OMESEC


General Information