Naproxen - 55154-0727-0 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 55154-0727
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 500    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 55154-0727
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074410
Marketing Category: ANDA
Start Marketing Date: 20091120

Package Information of Naproxen

Package NDC: 55154-0727-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0727-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Naproxen

NDC Code 55154-0727-0
Proprietary Name Naproxen
Package Description 10 BLISTER PACK in 1 BAG (55154-0727-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0727
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091120
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name NAPROXEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen


General Information