Celecoxib

Product NDC
80425-0321
11-digit product format
804250321
Labeler code
80425
Product ID
80425-0321_2a9ba8f4-6cf0-e827-e063-6394a90a0300
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Celecoxib
Dosage form
CAPSULE
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA210071
Marketing category
ANDA
Marketing start
2023-04-10
Substance
CELECOXIB
Active strength
100 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
80425-0321-18042503210130 CAPSULE in 1 BOTTLE (80425-0321-1) 30 capsule2023-04-10NoNoHistorical
80425-0321-28042503210260 CAPSULE in 1 BOTTLE (80425-0321-2) 60 capsule2023-04-10NoNoHistorical
80425-0321-38042503210390 CAPSULE in 1 BOTTLE (80425-0321-3) 90 capsule2023-04-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Celecoxib CapsulesAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2