NAPROXEN - 0143-9908-05 - (naproxen sodium)

Alphabetical Index


Drug Information of NAPROXEN

Product NDC: 0143-9908
Proprietary Name: NAPROXEN
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

Product NDC: 0143-9908
Labeler Name: West-Ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074480
Marketing Category: ANDA
Start Marketing Date: 19960514

Package Information of NAPROXEN

Package NDC: 0143-9908-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9908-05)

NDC Information of NAPROXEN

NDC Code 0143-9908-05
Proprietary Name NAPROXEN
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9908-05)
Product NDC 0143-9908
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name naproxen sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19960514
Marketing Category Name ANDA
Labeler Name West-Ward Pharmaceutical Corp
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


General Information