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United States · US · US:16103-381_fcbabd90-abc6-4a05-8841-58cb74b5a22e
PHARBINEX-DM
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharbest Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1116103381041 BOTTLE, PLASTIC in 1 CARTON (16103-381-04) / 30 TABLET in 1 BOTTLE, PLASTIC
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": {
"8d71db43-da87-45ee-aa4a-7e870bc5016d": {
"match": "brand_token",
"title": "PHARBINEX-DM (GUAIFENESIN 400MG AND DEXTROMETHORPHAN HBR 20MG) TABLET [PHARBEST PHARMACEUTICALS, INC.]",
"spl_version": "3",
"published_date": "2025-12-26"
}
},
"productid": "16103-381_fcbabd90-abc6-4a05-8841-58cb74b5a22e",
"productndc": "16103-381",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "PHARBINEX-DM",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "GUAIFENESIN 400mg and DEXTROMETHORPHAN HBR 20MG",
"start_marketing_date": "20180402",
"active_numerator_strength": "20; 400"
}Related drugs
Other records sharing ATC code R05DA.
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