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United States · US · US:50991-736_1cda79a6-71f0-4793-e063-6394a90a9a8a
Deconex IR
UNIISPLATC R05CA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPoly Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeR05CA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11509917360212 BLISTER PACK in 1 CARTON (50991-736-02) / 2 TABLET in 1 BLISTER PACK
- ndc1150991736901 BOTTLE in 1 CARTON (50991-736-90) / 90 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
495W7451VQ
GUAIFENESIN
RxCUI 5032
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "495W7451VQ",
"rxcui": "5032",
"inchikey": "HSRJKNPTNIJEKV-UHFFFAOYSA-N",
"display_name": "GUAIFENESIN",
"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": "50991-736_1cda79a6-71f0-4793-e063-6394a90a9a8a",
"productndc": "50991-736",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
"proprietary_name": "Deconex IR",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin and Phenylephrine HCl",
"start_marketing_date": "20160808",
"active_numerator_strength": "385; 10"
}Related drugs
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