"55513-508-55" National Drug Code (NDC)

Otezla 1 KIT in 1 BLISTER PACK (55513-508-55) * 4 TABLET, FILM COATED in 1 BLISTER PACK (55513-518-04) * 51 TABLET, FILM COATED in 1 BLISTER PACK (55513-497-51)
(Amgen Inc)

NDC Code55513-508-55
Package Description1 KIT in 1 BLISTER PACK (55513-508-55) * 4 TABLET, FILM COATED in 1 BLISTER PACK (55513-518-04) * 51 TABLET, FILM COATED in 1 BLISTER PACK (55513-497-51)
Product NDC55513-508
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOtezla
Non-Proprietary NameApremilast
Dosage FormKIT
Start Marketing Date20240427
Marketing Category NameNDA
Application NumberNDA205437
ManufacturerAmgen Inc

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