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Naproxen Sodium - 52605-144-24 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 52605-144
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 220    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 52605-144
Labeler Name: Polygen Pharmaceuticals LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA090545
Marketing Category: ANDA
Start Marketing Date: 20121113

Package Information of Naproxen Sodium

Package NDC: 52605-144-24
Package Description: 1 BOTTLE in 1 CARTON (52605-144-24) > 24 TABLET, COATED in 1 BOTTLE

NDC Information of Naproxen Sodium

NDC Code 52605-144-24
Proprietary Name Naproxen Sodium
Package Description 1 BOTTLE in 1 CARTON (52605-144-24) > 24 TABLET, COATED in 1 BOTTLE
Product NDC 52605-144
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121113
Marketing Category Name ANDA
Labeler Name Polygen Pharmaceuticals LLC
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Naproxen Sodium


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