pain relief

Generic: ibuprofen

Labeler: meijer, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief
Generic Name ibuprofen
Labeler meijer, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Meijer, Inc.

Identifiers & Regulatory

Product NDC 79481-0423
Product ID 79481-0423_65d1d017-6a03-477d-bb35-98d606a8036c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA072096
Listing Expiration 2026-12-31
Marketing Start 2024-07-15

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 794810423
Hyphenated Format 79481-0423

Supplemental Identifiers

RxCUI
310965
UNII
WK2XYI10QM
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 pain relief (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
  • 1 BOTTLE in 1 CARTON (79481-0423-0) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (79481-0423-1) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 500 TABLET, FILM COATED in 1 BOTTLE (79481-0423-2)
  • 1 BOTTLE in 1 CARTON (79481-0423-3) / 100 TABLET, FILM COATED in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (79481-0423-4) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (5)

79481-0423-0 1 BOTTLE in 1 CARTON (79481-0423-0) / 24 TABLET, FILM COATED in 1 BOTTLE 79481-0423-1 1 BOTTLE in 1 CARTON (79481-0423-1) / 50 TABLET, FILM COATED in 1 BOTTLE 79481-0423-2 500 TABLET, FILM COATED in 1 BOTTLE (79481-0423-2) 79481-0423-3 1 BOTTLE in 1 CARTON (79481-0423-3) / 100 TABLET, FILM COATED in 1 BOTTLE 79481-0423-4 2 BOTTLE in 1 CARTON (79481-0423-4) / 100 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

pain relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "65d1d017-6a03-477d-bb35-98d606a8036c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["ae39917e-1998-4298-8686-919c0d3c2b07"], "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": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0423-0)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79481-0423-0", "marketing_start_date": "20240826"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0423-1)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79481-0423-1", "marketing_start_date": "20240805"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (79481-0423-2)", "package_ndc": "79481-0423-2", "marketing_start_date": "20240930"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79481-0423-3)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79481-0423-3", "marketing_start_date": "20240715"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (79481-0423-4)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79481-0423-4", "marketing_start_date": "20240722"}], "brand_name": "pain relief", "product_id": "79481-0423_65d1d017-6a03-477d-bb35-98d606a8036c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79481-0423", "generic_name": "Ibuprofen", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20240715", "listing_expiration_date": "20261231"}