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Naproxen Sodium - 57344-145-01 - (NAPROXEN SODIUM)

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Drug Information of Naproxen Sodium

Product NDC: 57344-145
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: 57344-145
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079096
Marketing Category: ANDA
Start Marketing Date: 20121215

Package Information of Naproxen Sodium

Package NDC: 57344-145-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Naproxen Sodium

NDC Code 57344-145-01
Proprietary Name Naproxen Sodium
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 57344-145
Product Type Name HUMAN OTC DRUG
Non Proprietary Name NAPROXEN SODIUM
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20121215
Marketing Category Name ANDA
Labeler Name AAA Pharmaceutical, Inc.
Substance Name NAPROXEN SODIUM
Strength Number 220
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Naproxen Sodium


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