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Naproxen Sodium - 68788-9881-2 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 68788-9881
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen Sodium

Product NDC: 68788-9881
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074661
Marketing Category: ANDA
Start Marketing Date: 20120312

Package Information of Naproxen Sodium

Package NDC: 68788-9881-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (68788-9881-2)

NDC Information of Naproxen Sodium

NDC Code 68788-9881-2
Proprietary Name Naproxen Sodium
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (68788-9881-2)
Product NDC 68788-9881
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120312
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Naproxen Sodium


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