Naprelan - 59630-777-03 - (Naproxen Sodium)

Alphabetical Index


Drug Information of Naprelan

Product NDC: 59630-777
Proprietary Name: Naprelan
Non Proprietary Name: Naproxen Sodium
Active Ingredient(s): 750    mg/1 & nbsp;   Naproxen Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Naprelan

Product NDC: 59630-777
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020353
Marketing Category: NDA
Start Marketing Date: 19960401

Package Information of Naprelan

Package NDC: 59630-777-03
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59630-777-03)

NDC Information of Naprelan

NDC Code 59630-777-03
Proprietary Name Naprelan
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59630-777-03)
Product NDC 59630-777
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Naproxen Sodium
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19960401
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name NAPROXEN SODIUM
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of Naprelan


General Information