ibuprofen

Generic: ibuprofen

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-357
Product ID 71205-357_c18cb763-af0c-4cc2-b7df-520835c91884
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2026-12-31
Marketing Start 2018-09-20

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 71205357
Hyphenated Format 71205-357

Supplemental Identifiers

RxCUI
310965
UPC
0371205357603
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA072096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)
  • 24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30)
  • 50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)
source: ndc

Packages (6)

71205-357-06 6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06) 71205-357-24 24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24) 71205-357-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30) 71205-357-50 50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50) 71205-357-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60) 71205-357-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c18cb763-af0c-4cc2-b7df-520835c91884", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205357603"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["798d33b0-5d7a-4445-8a51-2a3d336f744a"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)", "package_ndc": "71205-357-06", "marketing_start_date": "20191112"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)", "package_ndc": "71205-357-24", "marketing_start_date": "20210826"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30)", "package_ndc": "71205-357-30", "marketing_start_date": "20191112"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50)", "package_ndc": "71205-357-50", "marketing_start_date": "20191112"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60)", "package_ndc": "71205-357-60", "marketing_start_date": "20191112"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)", "package_ndc": "71205-357-90", "marketing_start_date": "20191112"}], "brand_name": "ibuprofen", "product_id": "71205-357_c18cb763-af0c-4cc2-b7df-520835c91884", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-357", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20180920", "listing_expiration_date": "20261231"}