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United States · US · US:42507-222_8e6a9cf0-fcd0-46b2-a984-2b328b55af07
MUCUS DM
Orange BookUNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHyVee Inc
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1142507222201 BOTTLE in 1 CARTON (42507-222-20) / 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (42507-222-01)
Annotations
UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
Orange Book
A207602
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9D2RTI9KYH",
"rxcui": "102490",
"inchikey": "STTADZBLEUMJRG-IKNOHUQMSA-N",
"display_name": "DEXTROMETHORPHAN HYDROBROMIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"84b5d83d-aea5-42ed-b20c-96d3b389c8c0": {
"match": "brand_token",
"title": "MUCUS RELIEF DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) TABLET, EXTENDED RELEASE [RITE AID CORPORATION]",
"spl_version": "3",
"published_date": "2026-05-28"
}
},
"productid": "42507-222_8e6a9cf0-fcd0-46b2-a984-2b328b55af07",
"productndc": "42507-222",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "207602",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "60MG;1.2GM",
"product_no": "001",
"approval_date": "Mar 5, 2018"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "30MG;600MG",
"product_no": "002",
"approval_date": "Mar 5, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "MUCUS DM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA207602",
"marketing_category": "ANDA",
"nonproprietary_name": "dextromethorphan hydrobromide, guaifenesin",
"start_marketing_date": "20260225",
"active_numerator_strength": "30; 600"
}Related drugs
Other records sharing ATC code R05DA.
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