motrin ib
Generic: ibuprofen
Labeler: kenvue brands llcDrug Facts
Product Profile
Brand Name
motrin ib
Generic Name
ibuprofen
Labeler
kenvue brands llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ibuprofen 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50580-230
Product ID
50580-230_4003a46c-d99c-72f4-e063-6394a90ab2db
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA077349
Listing Expiration
2026-12-31
Marketing Start
2016-07-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50580230
Hyphenated Format
50580-230
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
motrin ib (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA077349 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (50580-230-01) / 50 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-02) / 60 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-03) / 100 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-04) / 225 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-05) / 300 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-06) / 500 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (50580-230-07) / 24 TABLET, FILM COATED in 1 BOTTLE
- 2 TABLET, FILM COATED in 1 POUCH (50580-230-08)
- 50 POUCH in 1 CARTON (50580-230-09) / 2 TABLET, FILM COATED in 1 POUCH
Packages (9)
50580-230-01
1 BOTTLE in 1 CARTON (50580-230-01) / 50 TABLET, FILM COATED in 1 BOTTLE
50580-230-02
1 BOTTLE in 1 CARTON (50580-230-02) / 60 TABLET, FILM COATED in 1 BOTTLE
50580-230-03
1 BOTTLE in 1 CARTON (50580-230-03) / 100 TABLET, FILM COATED in 1 BOTTLE
50580-230-04
1 BOTTLE in 1 CARTON (50580-230-04) / 225 TABLET, FILM COATED in 1 BOTTLE
50580-230-05
1 BOTTLE in 1 CARTON (50580-230-05) / 300 TABLET, FILM COATED in 1 BOTTLE
50580-230-06
1 BOTTLE in 1 CARTON (50580-230-06) / 500 TABLET, FILM COATED in 1 BOTTLE
50580-230-07
1 BOTTLE in 1 CARTON (50580-230-07) / 24 TABLET, FILM COATED in 1 BOTTLE
50580-230-08
2 TABLET, FILM COATED in 1 POUCH (50580-230-08)
50580-230-09
50 POUCH in 1 CARTON (50580-230-09) / 2 TABLET, FILM COATED in 1 POUCH
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4003a46c-d99c-72f4-e063-6394a90ab2db", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0300450481269"], "unii": ["WK2XYI10QM"], "rxcui": ["201126", "310965"], "spl_set_id": ["d21129f8-4d96-4e36-bc39-a534306dd77e"], "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": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-01) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-01", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-02) / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-02", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-03) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-03", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-04) / 225 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-04", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-05) / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-05", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-06) / 500 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-06", "marketing_start_date": "20160701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-230-07) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-230-07", "marketing_start_date": "20170717"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 POUCH (50580-230-08)", "package_ndc": "50580-230-08", "marketing_start_date": "20170630"}, {"sample": false, "description": "50 POUCH in 1 CARTON (50580-230-09) / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "50580-230-09", "marketing_start_date": "20170424"}], "brand_name": "Motrin IB", "product_id": "50580-230_4003a46c-d99c-72f4-e063-6394a90ab2db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50580-230", "generic_name": "Ibuprofen", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motrin IB", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA077349", "marketing_category": "ANDA", "marketing_start_date": "20160701", "listing_expiration_date": "20261231"}