Naproxen - 53808-0739-1 - (NAPROXEN)

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Drug Information of Naproxen

Product NDC: 53808-0739
Proprietary Name: Naproxen
Non Proprietary Name: NAPROXEN
Active Ingredient(s): 500    mg/1 & nbsp;   NAPROXEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Naproxen

Product NDC: 53808-0739
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074201
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Naproxen

Package NDC: 53808-0739-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0739-1)

NDC Information of Naproxen

NDC Code 53808-0739-1
Proprietary Name Naproxen
Package Description 30 TABLET in 1 BLISTER PACK (53808-0739-1)
Product NDC 53808-0739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NAPROXEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name NAPROXEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naproxen


General Information