Naproxen - 63874-301-30 - (Naproxen)

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Drug Information of Naproxen

Product NDC: 63874-301
Proprietary Name: Naproxen
Non Proprietary Name: Naproxen
Active Ingredient(s): 250    mg/1 & nbsp;   Naproxen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 63874-301
Labeler Name: Altura Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078250
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Naproxen

Package NDC: 63874-301-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (63874-301-30)

NDC Information of Naproxen

NDC Code 63874-301-30
Proprietary Name Naproxen
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (63874-301-30)
Product NDC 63874-301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name Altura Pharmaceuticals, Inc.
Substance Name NAPROXEN
Strength Number 250
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