ibuprofen

Generic: ibuprofen

Labeler: retail business services , llc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler retail business services , llc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
RETAIL BUSINESS SERVICES , LLC.

Identifiers & Regulatory

Product NDC 72476-110
Product ID 72476-110_43e187f3-1464-22f3-e063-6394a90a1135
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079174
Listing Expiration 2026-12-31
Marketing Start 2020-02-01

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 72476110
Hyphenated Format 72476-110

Supplemental Identifiers

RxCUI
310965
UPC
0341520310508
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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA079174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-110-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 PACKAGE in 1 CARTON (72476-110-03) / 100 TABLET, COATED in 1 PACKAGE
  • 1 BOTTLE, PLASTIC in 1 CARTON (72476-110-04) / 250 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 500 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-110-05)
source: ndc

Packages (4)

72476-110-02 1 BOTTLE, PLASTIC in 1 CARTON (72476-110-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 72476-110-03 1 PACKAGE in 1 CARTON (72476-110-03) / 100 TABLET, COATED in 1 PACKAGE 72476-110-04 1 BOTTLE, PLASTIC in 1 CARTON (72476-110-04) / 250 TABLET, COATED in 1 BOTTLE, PLASTIC 72476-110-05 500 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-110-05)

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": "43e187f3-1464-22f3-e063-6394a90a1135", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0341520310508"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8f9f308f-0ca5-12fa-e053-2995a90a47fc"], "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": ["RETAIL BUSINESS SERVICES , LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-110-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72476-110-02", "marketing_start_date": "20201101"}, {"sample": false, "description": "1 PACKAGE in 1 CARTON (72476-110-03)  / 100 TABLET, COATED in 1 PACKAGE", "package_ndc": "72476-110-03", "marketing_start_date": "20200201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72476-110-04)  / 250 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72476-110-04", "marketing_start_date": "20200201"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE, PLASTIC (72476-110-05)", "package_ndc": "72476-110-05", "marketing_start_date": "20200201"}], "brand_name": "Ibuprofen", "product_id": "72476-110_43e187f3-1464-22f3-e063-6394a90a1135", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72476-110", "generic_name": "Ibuprofen", "labeler_name": "RETAIL BUSINESS SERVICES , LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA079174", "marketing_category": "ANDA", "marketing_start_date": "20200201", "listing_expiration_date": "20261231"}