ibuprofen

Generic: ibuprofen

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

ibuprofen 800 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-266
Product ID 72189-266_2c285455-94b8-8154-e063-6394a90a0e8c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090796
Listing Expiration 2026-12-31
Marketing Start 2021-09-16

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 72189266
Hyphenated Format 72189-266

Supplemental Identifiers

RxCUI
197806 197807
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 ANDA090796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30)
  • 40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40)
  • 60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60)
  • 100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71)
  • 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)
source: ndc

Packages (7)

72189-266-15 15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15) 72189-266-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30) 72189-266-40 40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40) 72189-266-60 60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60) 72189-266-71 100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71) 72189-266-72 120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72) 72189-266-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)

Ingredients (1)

ibuprofen (800 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": "2c285455-94b8-8154-e063-6394a90a0e8c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197806", "197807"], "spl_set_id": ["c3f30813-0848-6e8a-e053-2995a90a3dea"], "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": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15)", "package_ndc": "72189-266-15", "marketing_start_date": "20210916"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30)", "package_ndc": "72189-266-30", "marketing_start_date": "20210916"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40)", "package_ndc": "72189-266-40", "marketing_start_date": "20210916"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60)", "package_ndc": "72189-266-60", "marketing_start_date": "20210916"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71)", "package_ndc": "72189-266-71", "marketing_start_date": "20210916"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72)", "package_ndc": "72189-266-72", "marketing_start_date": "20210916"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)", "package_ndc": "72189-266-90", "marketing_start_date": "20210916"}], "brand_name": "IBUPROFEN", "product_id": "72189-266_2c285455-94b8-8154-e063-6394a90a0e8c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-266", "generic_name": "IBUPROFEN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20210916", "listing_expiration_date": "20261231"}