Celecoxib

Product NDC
72162-2175
11-digit product format
721622175
Labeler code
72162
Product ID
72162-2175_b65f5ec1-7f05-4505-b07d-4dc28a80306b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA205129
Marketing category
ANDA
Marketing start
2020-12-03
Substance
CELECOXIB
Active strength
200 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
JCX84Q7J1LCELECOXIB169590-42-5CELECOXIB

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-2175-37216221750330 CAPSULE in 1 BOTTLE (72162-2175-3) 30 capsule2023-12-07NoNoHistorical
72162-2175-572162217505500 CAPSULE in 1 BOTTLE (72162-2175-5) 500 capsule2023-12-07NoNoHistorical
72162-2175-67216221750660 CAPSULE in 1 BOTTLE (72162-2175-6) 60 capsule2023-12-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CelecoxibBryant Ranch Prepack2024-11-07HUMAN PRESCRIPTION DRUG LABEL102