43598-430 : Dimethyl Fumarate 240 mg Oral Capsule, Delayed Release

NDC:	43598-430
Labeler:	Dr. Reddy's Laboratories Inc.
Product Type:	Human Prescription Drug
Drug Name:	Dimethyl Fumarate
Dosage Form:	Oral Capsule, Delayed Release
Application #:	ANDA210460
Rev. Date:	Sep 28, 2020

^[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

• 43853-0021-1: 30 ML IN 1 BOTTLE, SPRAY (43853‑0021‑1)

Active Ingredients:

• Avena Sativa Flowering Top
• Barium Carbonate
• Milk Thistle
• Turnera Diffusa Leafy Twig
• Hamamelis Virginiana Root Bark/Stem Bark
• Pork Liver
• Asian Ginseng
• Nuphar Lutea Root
• Sus Scrofa Testicle
• Phosphoric Acid
• Populus Tremuloides Leaf
• Saw Palmetto
• Selenium
• Testosterone

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