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"31722-087-31" National Drug Code (NDC)

Apremilast 1 BLISTER PACK in 1 CARTON (31722-087-31) / 1 KIT in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK * 19 TABLET, FILM COATED in 1 BLISTER PACK
(Camber Pharmaceuticals, Inc.)

NDC Code31722-087-31
Package Description1 BLISTER PACK in 1 CARTON (31722-087-31) / 1 KIT in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK * 19 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC31722-087
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameApremilast
Non-Proprietary NameApremilast
Dosage FormKIT
Start Marketing Date20230726
Marketing Category NameANDA
Application NumberANDA211878
ManufacturerCamber Pharmaceuticals, Inc.

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