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Naproxen Sodium - 52959-271-02 - (Naproxen)

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Drug Information of Naproxen Sodium

Product NDC: 52959-271
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen
Active Ingredient(s): 550    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 52959-271
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078250
Marketing Category: ANDA
Start Marketing Date: 20070701

Package Information of Naproxen Sodium

Package NDC: 52959-271-02
Package Description: 200 TABLET in 1 VIAL, PLASTIC (52959-271-02)

NDC Information of Naproxen Sodium

NDC Code 52959-271-02
Proprietary Name Naproxen Sodium
Package Description 200 TABLET in 1 VIAL, PLASTIC (52959-271-02)
Product NDC 52959-271
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070701
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name NAPROXEN SODIUM
Strength Number 550
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen Sodium


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