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United States · US · US:0363-1144_6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a
tussin dm max
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWalgreen Company
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1103631144261 BOTTLE in 1 CARTON (0363-1144-26) / 118 mL in 1 BOTTLE
- ndc1103631144341 BOTTLE in 1 CARTON (0363-1144-34) / 237 mL in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
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": {
"e1280355-da81-489f-9bd2-ffea9a68010c": {
"match": "brand_token",
"title": "TUSSIN COUGH AND CHEST CONGESTION DM ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [HARRIS TEETER, LLC]",
"spl_version": "3",
"published_date": "2026-04-30"
}
},
"productid": "0363-1144_6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a",
"productndc": "0363-1144",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "tussin dm max",
"active_ingred_unit": "mg/20mL; mg/20mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Dextromethorphan Hydrobromide, Guaifenesin",
"start_marketing_date": "20220524",
"active_numerator_strength": "20; 400"
}Related drugs
Other records sharing ATC code R05DA.
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