Otezla

Product NDC
55513-996
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
apremilast
Dosage form
KIT
Labeler
Amgen, Inc
Application
NDA205437
Marketing category
NDA
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55513-996-953 BLISTER PACK in 1 CARTON (55513-996-95) / 1 KIT in 1 BLISTER PACK (55513-996-96) * 4 TABLET, FILM COATED in 1 BLISTER PACK (55513-518-04) * 23 TABLET, FILM COATED in 1 BLISTER PACK (55513-497-23) 2024-04-27NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
OtezlaAmgen, Inc | Celgene International Sarl2025-12-23HUMAN PRESCRIPTION DRUG LABEL34