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United States · US · US:67414-240_ddd2849e-23ea-dd00-e053-2995a90a252f
Motrin IB
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerJones Healthcare Group - Packaging Services, Inc
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1167414240002500 POUCH in 1 BOX (67414-240-00) / 2 TABLET, FILM COATED in 1 POUCH
- ndc11674142400950 POUCH in 1 CARTON (67414-240-09) / 2 TABLET, FILM COATED in 1 POUCH
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A077349
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WK2XYI10QM",
"rxcui": "5640",
"inchikey": "HEFNNWSXXWATRW-UHFFFAOYSA-N",
"display_name": "IBUPROFEN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c57f6ded-c0bd-45ae-823a-4c02ce334d98": {
"match": "brand_token",
"title": "MOTRIN INFANTS (IBUPROFEN) SUSPENSION/ DROPS [KENVUE BRANDS LLC]",
"spl_version": "17",
"published_date": "2026-05-20"
}
},
"productid": "67414-240_ddd2849e-23ea-dd00-e053-2995a90a252f",
"productndc": "67414-240",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "077349",
"products": [
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Jun 21, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Motrin IB",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077349",
"marketing_category": "ANDA",
"nonproprietary_name": "IBUPROFEN",
"start_marketing_date": "20160701",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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