Naproxen - 0143-1348-05 - (Naproxen)

Alphabetical Index


Drug Information of Naproxen

Product NDC: 0143-1348
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: 0143-1348
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076494
Marketing Category: ANDA
Start Marketing Date: 20040114

Package Information of Naproxen

Package NDC: 0143-1348-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0143-1348-05)

NDC Information of Naproxen

NDC Code 0143-1348-05
Proprietary Name Naproxen
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0143-1348-05)
Product NDC 0143-1348
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040114
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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