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Lansoprazole - 64679-669-06 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 64679-669
Proprietary Name: Lansoprazole
Non Proprietary Name: Lansoprazole
Active Ingredient(s): 15    mg/1 & nbsp;   Lansoprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Lansoprazole

Product NDC: 64679-669
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202176
Marketing Category: ANDA
Start Marketing Date: 20120810

Package Information of Lansoprazole

Package NDC: 64679-669-06
Package Description: 10 BLISTER PACK in 1 CARTON (64679-669-06) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Lansoprazole

NDC Code 64679-669-06
Proprietary Name Lansoprazole
Package Description 10 BLISTER PACK in 1 CARTON (64679-669-06) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 64679-669
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120810
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Lansoprazole


General Information