LODINE (Page 6 of 6)

PRINCIPAL DISPLAY PANEL

400 mg Bottle Label

NDC 69036-503-30

30 Tablets

Lodine
Tablets USP,
400 mg

Sealed for your protection

Sallus Laboratories, LLC Rx only

PRINCIPAL DISPLAY PANEL -- 400 mg Bottle Label 

NDC 69036-503-30

30 Tablets

Lodine 
Tablets USP, 
400 mg

Sealed for your protection

Sallus Laboratories, LLC
Rx only
(click image for full-size original)
LODINE etodolac tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69036-503
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ETODOLAC (ETODOLAC) ETODOLAC 400 mg
Inactive Ingredients
Ingredient Name Strength
HYPROMELLOSE 2208 (15000 MPA.S)
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOLS
POVIDONE
SODIUM STARCH GLYCOLATE TYPE A POTATO
TITANIUM DIOXIDE
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
Product Characteristics
Color ORANGE (peach colored) Score no score
Shape OVAL Size 19mm
Flavor Imprint Code T88
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69036-503-30 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075074 09/01/2016
Labeler — Sallus Laboratories, LLC (079418254)

Revised: 10/2016 Sallus Laboratories, LLC

All MedLibrary.org resources are included in as near-original form as possible, meaning that the information from the original provider has been rendered here with only typographical or stylistic modifications and not with any substantive alterations of content, meaning or intent.

This site is provided for educational and informational purposes only, in accordance with our Terms of Use, and is not intended as a substitute for the advice of a medical doctor, nurse, nurse practitioner or other qualified health professional.

Privacy Policy | Copyright © 2022. All Rights Reserved.