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Naproxen Sodium - 35356-748-14 - (Naproxen Sodium)

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Drug Information of Naproxen Sodium

Product NDC: 35356-748
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: 35356-748
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074198
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of Naproxen Sodium

Package NDC: 35356-748-14
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE (35356-748-14)

NDC Information of Naproxen Sodium

NDC Code 35356-748-14
Proprietary Name Naproxen Sodium
Package Description 14 TABLET, FILM COATED in 1 BOTTLE (35356-748-14)
Product NDC 35356-748
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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