CELECOXIB

Product NDC
50090-6758
11-digit product format
500906758
Labeler code
50090
Product ID
50090-6758_68d04fdf-19cc-41f2-afb0-c03105469a52
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CELECOXIB
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA207446
Marketing category
ANDA
Marketing start
2017-09-26
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
50090-6758-05009067580030 CAPSULE in 1 BOTTLE (50090-6758-0) 30 capsule2023-10-17NoNoHistorical
50090-6758-15009067580160 CAPSULE in 1 BOTTLE (50090-6758-1) 60 capsule2023-10-17NoNoHistorical
50090-6758-25009067580290 CAPSULE in 1 BOTTLE (50090-6758-2) 90 capsule2023-10-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CELECOXIBA-S Medication Solutions2025-05-30HUMAN PRESCRIPTION DRUG LABEL3