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United States · US · US:50991-740_1cda4e52-f3cb-04b3-e063-6394a90a863f
DECONEX
UNIISPLATC R05DA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPoly Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeR05DA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc115099174001100 TABLET in 1 BOTTLE (50991-740-01)
- ndc11509917400212 BLISTER PACK in 1 CARTON (50991-740-02) / 1 TABLET in 1 BLISTER PACK
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": {
"8aab8e5c-1633-2e5a-e053-2a95a90adcc5": {
"match": "brand_token",
"title": "DECONEX DMX (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE) TABLET [POLY PHARMACEUTICALS, INC.]",
"spl_version": "6",
"published_date": "2024-07-11"
}
},
"productid": "50991-740_1cda4e52-f3cb-04b3-e063-6394a90a863f",
"productndc": "50991-740",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
"proprietary_name": "DECONEX",
"active_ingred_unit": "mg/1; mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride",
"start_marketing_date": "20190601",
"active_numerator_strength": "17.5; 400; 10"
}Related drugs
Other records sharing ATC code R05DA.
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