NDC 0025-1525

CELEBREX

Celecoxib

CELEBREX is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Celecoxib.

• Product ID: 0025-1525_41552700-8f2e-4ce8-a74a-a8db83266cd3
• NDC: 0025-1525
• Product Type: Human Prescription Drug
• Proprietary Name: CELEBREX
• Generic Name: Celecoxib
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1998-10-02
• Marketing Category: NDA / NDA
• Application Number: NDA020998
• Labeler Name: Pfizer Laboratories Div Pfizer Inc
• Substance Name: CELECOXIB
• Active Ingredient Strength: 200 mg/1
• Pharm Classes: Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 0025-1525-31

100 CAPSULE in 1 BOTTLE (0025-1525-31)

• Marketing Start Date: 1998-10-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0025-1525-31 [00025152531]

CELEBREX CAPSULE

• Marketing Category: NDA
• Application Number: NDA020998
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1998-10-02

NDC 0025-1525-51 [00025152551]

CELEBREX CAPSULE

• Marketing Category: NDA
• Application Number: NDA020998
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1998-10-02

NDC 0025-1525-96 [00025152596]

CELEBREX CAPSULE

• Marketing Category: NDA
• Application Number: NDA020998
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1998-10-02

NDC 0025-1525-34 [00025152534]

CELEBREX CAPSULE

• Marketing Category: NDA
• Application Number: NDA020998
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1998-10-02

NDC 0025-1525-99 [00025152599]

CELEBREX CAPSULE

• Marketing Category: NDA
• Application Number: NDA020998
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-10-06

Drug Details

Active Ingredients

Ingredient	Strength
CELECOXIB	200 mg/1

OpenFDA Data

• SPL SET ID: 8d52185d-421f-4e34-8db7-f7676db2a226
• Manufacturer:
  • G.D. Searle LLC Division of Pfizer Inc
• UNII:
  • JCX84Q7J1L
• RxNorm Concept Unique ID - RxCUI:
  • 349514
  • 686381
  • 686379
  • 213468
  • 213469
  • 352314
  • 205323
  • 205322
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• UPC Code:
  • 0300251520310
  • 0300251515019
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721

Pharmacological Class

• Cyclooxygenase Inhibitors [MoA]
• Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient]
• Nonsteroidal Anti-inflammatory Drug [EPC]

NDC Crossover Matching brand name "CELEBREX" or generic name "Celecoxib"

NDC	Brand Name	Generic Name
0025-1515	CELEBREX	Celecoxib
0025-1520	CELEBREX	Celecoxib
0025-1525	CELEBREX	Celecoxib
0025-1530	CELEBREX	Celecoxib
68387-552	CELEBREX	CELEBREX
68788-0768	CELEBREX	CELEBREX
21695-023	CELEBREX	CELEBREX
21695-022	CELEBREX	CELEBREX
33261-019	CELEBREX	CELEBREX
49999-383	CELEBREX	CELEBREX
52959-540	CELEBREX	CELEBREX
52959-539	CELEBREX	CELEBREX
55154-3621	CELEBREX	CELEBREX
55154-3622	CELEBREX	CELEBREX
55289-451	CELEBREX	CELEBREX
55154-3625	CELEBREX	CELEBREX
55289-475	CELEBREX	CELEBREX
61919-046	CELEBREX	CELEBREX
63187-079	CELEBREX	CELEBREX
63629-6368	CELEBREX	CELEBREX
63629-3021	CELEBREX	CELEBREX
66336-940	CELEBREX	CELEBREX
67544-204	CELEBREX	CELEBREX
80425-0096	Celebrex	Celebrex
80425-0038	Celebrex	Celebrex
80425-0040	Celebrex	Celebrex
80425-0037	Celebrex	Celebrex
80425-0039	Celebrex	Celebrex
0093-7165	Celecoxib	Celecoxib
0093-7166	Celecoxib	Celecoxib
0093-7170	Celecoxib	Celecoxib
0093-7306	Celecoxib	Celecoxib