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Naproxen Sodium - 65862-516-01 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 65862-516
Proprietary Name: Naproxen Sodium
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 550    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: 65862-516
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200629
Marketing Category: ANDA
Start Marketing Date: 20111031

Package Information of Naproxen Sodium

Package NDC: 65862-516-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (65862-516-01)

NDC Information of Naproxen Sodium

NDC Code 65862-516-01
Proprietary Name Naproxen Sodium
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (65862-516-01)
Product NDC 65862-516
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111031
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name NAPROXEN SODIUM
Strength Number 550
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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