Naproxen - 52959-516-02 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 52959-516
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 500    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 52959-516
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075227
Marketing Category: ANDA
Start Marketing Date: 20100923

Package Information of Naproxen

Package NDC: 52959-516-02
Package Description: 120 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-516-02)

NDC Information of Naproxen

NDC Code 52959-516-02
Proprietary Name Naproxen
Package Description 120 TABLET, DELAYED RELEASE in 1 BOTTLE (52959-516-02)
Product NDC 52959-516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100923
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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