advil

Generic: ibuprofen

Labeler: navajo manufacturing company inc.
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name advil
Generic Name ibuprofen
Labeler navajo manufacturing company inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

Identifiers & Regulatory

Product NDC 67751-146
Product ID 67751-146_f70a8d20-570c-1e94-e053-6294a90ab66f
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA018989
Listing Expiration 2026-12-31
Marketing Start 2016-09-20

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 67751146
Hyphenated Format 67751-146

Supplemental Identifiers

RxCUI
153008 310965
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 advil (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number NDA018989 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 POUCH in 1 CARTON (67751-146-01) / 2 TABLET, COATED in 1 POUCH
  • 2 POUCH in 1 CARTON (67751-146-02) / 2 TABLET, COATED in 1 POUCH
source: ndc

Packages (2)

67751-146-01 1 POUCH in 1 CARTON (67751-146-01) / 2 TABLET, COATED in 1 POUCH 67751-146-02 2 POUCH in 1 CARTON (67751-146-02) / 2 TABLET, COATED in 1 POUCH

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Advil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f70a8d20-570c-1e94-e053-6294a90ab66f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["153008", "310965"], "spl_set_id": ["4a64522f-b7d8-47f7-bf07-c9e8f1086425"], "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": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (67751-146-01)  / 2 TABLET, COATED in 1 POUCH", "package_ndc": "67751-146-01", "marketing_start_date": "20160920"}, {"sample": false, "description": "2 POUCH in 1 CARTON (67751-146-02)  / 2 TABLET, COATED in 1 POUCH", "package_ndc": "67751-146-02", "marketing_start_date": "20160920"}], "brand_name": "Advil", "product_id": "67751-146_f70a8d20-570c-1e94-e053-6294a90ab66f", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67751-146", "generic_name": "IBUPROFEN", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Advil", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "NDA018989", "marketing_category": "NDA", "marketing_start_date": "20160920", "listing_expiration_date": "20261231"}