Celecoxib

Product NDC
68071-2733
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA205129
Marketing category
ANDA
Substance
CELECOXIB
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-2733-040 CAPSULE in 1 BOTTLE (68071-2733-0) 2022-05-25NoHistorical
68071-2733-330 CAPSULE in 1 BOTTLE (68071-2733-3) 2022-05-25NoHistorical
68071-2733-660 CAPSULE in 1 BOTTLE (68071-2733-6) 2022-05-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CelecoxibNuCare Pharmaceuticals,Inc.2024-08-05HUMAN PRESCRIPTION DRUG LABEL3