Dimethyl Fumarate 70512-0852

Product NDC

70512-0852

Manufacturer: Sola Pharmaceuticals, Llc
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 31, 2023
Listing Expires: December 31, 2026
Application: ANDA210436

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Active Ingredients

Ingredient	Strength
Dimethyl Fumarate	120 mg/1

Packaging Options(1)

70512-0852-14

1 BOTTLE in 1 CARTON (70512-852-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

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