Diclofenac Sodium (Page 8 of 8)

Diclofenac Sodium

Label ImageLabel Image
DICLOFENAC SODIUM diclofenac sodium gel
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50090-4020(NDC:69097-524)
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DICLOFENAC SODIUM (DICLOFENAC) DICLOFENAC SODIUM 10 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
COCO-CAPRYLATE/CAPRATE
ISOPROPYL ALCOHOL
MINERAL OIL
POLYOXYL 20 CETOSTEARYL ETHER
PROPYLENE GLYCOL
WATER
AMMONIA
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50090-4020-0 1 TUBE in 1 CARTON contains a TUBE
1 100 g in 1 TUBE This package is contained within the CARTON (50090-4020-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA209903 08/16/2018
Labeler — A-S Medication Solutions (830016429)
Establishment
Name Address ID/FEI Operations
A-S Medication Solutions 830016429 RELABEL (50090-4020)

Revised: 11/2022 A-S Medication Solutions

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 © 2023. All Rights Reserved.