Prescription Drug Name:
NAPROXEN SODIUM 220mg
ID:
2d78bd54-2edb-37a7-e054-00144ff88e88
Code:
34391-3
Active ingredient (in each tablet)
id: 2d7a7f6e-a67f-13f0-e054-00144ff8d46c
displayName: OTC – ACTIVE INGREDIENT SECTION
FDA Article Code: 55106-9
Purpose
id: 2d7a7f6e-a681-13f0-e054-00144ff8d46c
displayName: OTC – PURPOSE SECTION
FDA Article Code: 55105-1
Uses
id: 2d7a7f6e-a683-13f0-e054-00144ff8d46c
displayName: GERIATRIC USE SECTION
FDA Article Code: 34082-8
Directions
id: 2d7a7f6e-a687-13f0-e054-00144ff8d46c
displayName: INSTRUCTIONS FOR USE SECTION
FDA Article Code: 59845-8
Other information
id: 2d7a7f6e-a689-13f0-e054-00144ff8d46c
displayName: STORAGE AND HANDLING SECTION
FDA Article Code: 44425-7
Inactive ingredients
id: 2d7ac259-585d-6456-e054-00144ff88e88
displayName: INACTIVE INGREDIENT SECTION
FDA Article Code: 51727-6
Principal Display Panel
id: 2d7a7f6e-a68e-13f0-e054-00144ff8d46c
displayName: PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA Article Code: 51945-4