NAPROXEN SODIUM 220mg

/NAPROXEN SODIUM 220mg
NAPROXEN SODIUM 220mg2018-09-06T09:12:40+00:00

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