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United States · US · US:47682-609_3e5d4984-a2e6-a9fc-e063-6394a90a4396
Medi-First Plus Ibuprofen
Orange BookUNIISPLATC G02CC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUnifirst First Aid Corporation
CountryUS (United States)
ATC codeG02CC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11476826093350 PACKET in 1 BOX (47682-609-33) / 2 TABLET, FILM COATED in 1 PACKET
- ndc114768260948125 PACKET in 1 BOX (47682-609-48) / 2 TABLET, FILM COATED in 1 PACKET
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A075010
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": {
"49f04e5d-746d-cbe9-e063-6294a90a7e88": {
"match": "brand_token",
"title": "MEDI-FIRST HYDROCORTISONE 1 % ANTI-ITCH CREAM (HYDROCORTISONE) CREAM [UNIFIRST FIRST AID CORPORATION]",
"spl_version": "4",
"published_date": "2026-05-28"
}
},
"productid": "47682-609_3e5d4984-a2e6-a9fc-e063-6394a90a4396",
"productndc": "47682-609",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "075010",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG",
"product_no": "001",
"approval_date": "Mar 1, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN",
"proprietary_name": "Medi-First Plus Ibuprofen",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075010",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen",
"start_marketing_date": "20160201",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code G02CC01.
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