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United States · US · US:85722-0001_a2cca1a0-64ab-4650-beb5-1265425eac7b
DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKJD Pharma Private Limited
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc118572200014118 mL in 1 BOTTLE (85722-0001-4)
- ndc118572200016473 mL in 1 BOTTLE (85722-0001-6)
- ndc118572200018236 mL in 1 BOTTLE (85722-0001-8)
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": {
"4fde00af-3824-44f1-8a5f-d88518e0a8c8": {
"match": "brand_token",
"title": "DEXTROMETHORPHAN POLISTIREX SUSPENSION, EXTENDED RELEASE [AUROHEALTH LLC]",
"spl_version": "2",
"published_date": "2026-05-20"
}
},
"productid": "85722-0001_a2cca1a0-64ab-4650-beb5-1265425eac7b",
"productndc": "85722-0001",
"dosage_form": "SYRUP",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"proprietary_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN",
"active_ingred_unit": "mg/5mL; mg/5mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN",
"start_marketing_date": "20210201",
"active_numerator_strength": "10; 100"
}Related drugs
Other records sharing ATC code R05DA.
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