celecoxib

Generic: celecoxib

Labeler: yiling pharmaceutical, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name celecoxib
Generic Name celecoxib
Labeler yiling pharmaceutical, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

celecoxib 50 mg/1

Manufacturer
Yiling Pharmaceutical, Inc.

Identifiers & Regulatory

Product NDC 69117-0020
Product ID 69117-0020_4723852e-6cb6-442b-e063-6294a90a1b80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211412
Listing Expiration 2026-12-31
Marketing Start 2020-03-06

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 691170020
Hyphenated Format 69117-0020

Supplemental Identifiers

RxCUI
205322 205323 349514 686379
UPC
0369117002230 0369117002117 0369117002223 0369117002124 0369117002315 0369117002322 0369117002018 0369117002025 0369117002216 0369117002032 0369117002339 0369117002131
UNII
JCX84Q7J1L
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name celecoxib (source: ndc)
Generic Name celecoxib (source: ndc)
Application Number ANDA211412 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (69117-0020-1)
  • 100 CAPSULE in 1 BOTTLE (69117-0020-2)
  • 500 CAPSULE in 1 BOTTLE (69117-0020-3)
source: ndc

Packages (3)

69117-0020-1 60 CAPSULE in 1 BOTTLE (69117-0020-1) 69117-0020-2 100 CAPSULE in 1 BOTTLE (69117-0020-2) 69117-0020-3 500 CAPSULE in 1 BOTTLE (69117-0020-3)

Ingredients (1)

celecoxib (50 mg/1)

Linked Drug Pages (1)

Celecoxib ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4723852e-6cb6-442b-e063-6294a90a1b80", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0369117002230", "0369117002117", "0369117002223", "0369117002124", "0369117002315", "0369117002322", "0369117002018", "0369117002025", "0369117002216", "0369117002032", "0369117002339", "0369117002131"], "unii": ["JCX84Q7J1L"], "rxcui": ["205322", "205323", "349514", "686379"], "spl_set_id": ["43979279-867b-4303-8f30-fc58ae75a069"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Yiling Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (69117-0020-1)", "package_ndc": "69117-0020-1", "marketing_start_date": "20200306"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69117-0020-2)", "package_ndc": "69117-0020-2", "marketing_start_date": "20200306"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (69117-0020-3)", "package_ndc": "69117-0020-3", "marketing_start_date": "20200306"}], "brand_name": "Celecoxib", "product_id": "69117-0020_4723852e-6cb6-442b-e063-6294a90a1b80", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69117-0020", "generic_name": "Celecoxib", "labeler_name": "Yiling Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Celecoxib", "active_ingredients": [{"name": "CELECOXIB", "strength": "50 mg/1"}], "application_number": "ANDA211412", "marketing_category": "ANDA", "marketing_start_date": "20200306", "listing_expiration_date": "20261231"}