Dimethyl Fumarate 82009-0138

Product NDC

82009-0138

Manufacturer: Quallent Pharmaceuticals Health Llc
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 15, 2024
Listing Expires: December 31, 2026
Application: ANDA210500

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Active Ingredients

Ingredient	Strength
Dimethyl Fumarate	240 mg/1

Packaging Options(1)

82009-0138-60

1 BOTTLE in 1 CARTON (82009-138-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE

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