Mycophenolate Mofetil 31722-0879

Product NDC

31722-0879

Manufacturer: Camber Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 22, 2024
Listing Expires: December 31, 2027
Application: ANDA208119

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Active Ingredients

Ingredient	Strength
Mycophenolate Mofetil	500 mg/1

Drug Class

Antimetabolite Immunosuppressant [EPC]

Packaging Options(2)

31722-0879-01

100 TABLET, FILM COATED in 1 BOTTLE (31722-879-01)

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31722-0879-05

500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05)

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