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United States · US · US:73581-405_3ce33efd-e300-a7e2-e063-6394a90ad2c1
MUCUS RELIEF - DM
Orange BookUNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerYYBA CORP
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11735814059898 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)
Annotations
UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
Orange Book
A214781
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": "73581-405_3ce33efd-e300-a7e2-e063-6394a90ad2c1",
"productndc": "73581-405",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "214781",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "30MG;600MG",
"product_no": "001",
"approval_date": "Jul 1, 2021"
},
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "60MG;1.2GM",
"product_no": "002",
"approval_date": "Jul 1, 2021"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "MUCUS RELIEF - DM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "ANDA214781",
"marketing_category": "ANDA",
"nonproprietary_name": "Guaifenesin, Dextromethorphan HBr",
"start_marketing_date": "20250401",
"active_numerator_strength": "60; 1200"
}Related drugs
Other records sharing ATC code R05DA.
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