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Omeprazole Delayed-Release - 63304-445-01 - (Omeprazole)

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Drug Information of Omeprazole Delayed-Release

Product NDC: 63304-445
Proprietary Name: Omeprazole Delayed-Release
Non Proprietary Name: Omeprazole
Active Ingredient(s): 40    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole Delayed-Release

Product NDC: 63304-445
Labeler Name: Ranbaxy Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019810
Marketing Category: NDA
Start Marketing Date: 20080725

Package Information of Omeprazole Delayed-Release

Package NDC: 63304-445-01
Package Description: 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63304-445-01)

NDC Information of Omeprazole Delayed-Release

NDC Code 63304-445-01
Proprietary Name Omeprazole Delayed-Release
Package Description 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63304-445-01)
Product NDC 63304-445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080725
Marketing Category Name NDA
Labeler Name Ranbaxy Laboratories Inc.
Substance Name OMEPRAZOLE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole Delayed-Release


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