MedPath

Truemed Group LLC

CELECOXIB

Approved
Approval ID

e5e8d2fc-7527-8bd6-e053-2995a90a9ab3

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 10, 2022

Manufacturers
FDA

Truemed Group LLC

DUNS: 004154534

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

CELECOXIB

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code82922-026
Product Classification
G
Generic Name
CELECOXIB
Product Specifications
Route of AdministrationORAL
Effective DateAugust 10, 2022
FDA Product Classification

INGREDIENTS (1)

CELECOXIB N-DES(BENZENESULFONAMIDE)Active
Quantity: 200 mg in 1 1
Code: G5K9F2B76J
Classification: ACTIB

Drug Labeling Information

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOINC: 51945-4Updated: 9/17/2022

Caja

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