Celecoxib

Product NDC
71335-2220
11-digit product format
713352220
Labeler code
71335
Product ID
71335-2220_4c2347db-b9e2-4521-b094-35fc2e1d4070
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
71335-2220-07133522200015 CAPSULE in 1 BOTTLE (71335-2220-0) 15 capsule2024-12-11NoNoHistorical
71335-2220-17133522200130 CAPSULE in 1 BOTTLE (71335-2220-1) 30 capsule2023-08-15NoNoHistorical
71335-2220-27133522200260 CAPSULE in 1 BOTTLE (71335-2220-2) 60 capsule2023-08-16NoNoHistorical
71335-2220-37133522200390 CAPSULE in 1 BOTTLE (71335-2220-3) 90 capsule2023-08-25NoNoHistorical
71335-2220-47133522200414 CAPSULE in 1 BOTTLE (71335-2220-4) 14 capsule2023-08-22NoNoHistorical
71335-2220-57133522200520 CAPSULE in 1 BOTTLE (71335-2220-5) 20 capsule2023-08-21NoNoHistorical
71335-2220-67133522200610 CAPSULE in 1 BOTTLE (71335-2220-6) 10 capsule2023-11-20NoNoHistorical
71335-2220-771335222007180 CAPSULE in 1 BOTTLE (71335-2220-7) 180 capsule2024-12-11NoNoHistorical
71335-2220-87133522200828 CAPSULE in 1 BOTTLE (71335-2220-8) 28 capsule2024-10-23NoNoHistorical
71335-2220-97133522200956 CAPSULE in 1 BOTTLE (71335-2220-9) 56 capsule2024-12-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CelecoxibBryant Ranch Prepack2024-12-11HUMAN PRESCRIPTION DRUG LABEL103