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Naproxen Sodium - 55289-367-28 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 55289-367
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 550    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 55289-367
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078432
Marketing Category: ANDA
Start Marketing Date: 20070426

Package Information of Naproxen Sodium

Package NDC: 55289-367-28
Package Description: 28 TABLET in 1 BOTTLE, PLASTIC (55289-367-28)

NDC Information of Naproxen Sodium

NDC Code 55289-367-28
Proprietary Name Naproxen Sodium
Package Description 28 TABLET in 1 BOTTLE, PLASTIC (55289-367-28)
Product NDC 55289-367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070426
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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