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Naproxen Sodium - 63874-489-60 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 63874-489
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 275    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: 63874-489
Labeler Name: Altura Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078314
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Naproxen Sodium

Package NDC: 63874-489-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (63874-489-60)

NDC Information of Naproxen Sodium

NDC Code 63874-489-60
Proprietary Name Naproxen Sodium
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (63874-489-60)
Product NDC 63874-489
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name Altura Pharmaceuticals, Inc.
Substance Name NAPROXEN SODIUM
Strength Number 275
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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