🇺🇸
United States · US · US:0363-0423_28d9145e-3aa3-4a6e-97d4-591a5ff16be9
Ibuprofen and Pseudoephedrine Hydrochloride
Orange BookUNIISPLATC C01EB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWALGREEN COMPANY
CountryUS (United States)
ATC codeC01EB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11036304232120 TABLET, COATED in 1 BLISTER PACK (0363-0423-21)
- ndc11036304234140 TABLET, COATED in 1 BLISTER PACK (0363-0423-41)
Annotations
UNII (FDA Substance ID)
WK2XYI10QM
IBUPROFEN
RxCUI 5640
Orange Book
A074567
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": {
"aeee629b-255c-40d8-8e95-779aec00f723": {
"match": "brand_token",
"title": "IBUPROFEN TABLET [NORTHSTAR RX LLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "0363-0423_28d9145e-3aa3-4a6e-97d4-591a5ff16be9",
"productndc": "0363-0423",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "074567",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "200MG;30MG",
"product_no": "001",
"approval_date": "Apr 17, 2001"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE",
"proprietary_name": "Ibuprofen and Pseudoephedrine Hydrochloride",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA074567",
"marketing_category": "ANDA",
"nonproprietary_name": "Ibuprofen and Pseudoephedrine Hydrochloride",
"start_marketing_date": "20170801",
"active_numerator_strength": "200; 30"
}Related drugs
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