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United States · US · US:50991-212_26838be8-5a59-bb4d-e063-6394a90affe9
Poly-Vent 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
- ndc115099121201100 TABLET in 1 BOTTLE (50991-212-01)
- ndc11509912120212 TABLET in 1 BLISTER PACK (50991-212-02)
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": {
"739329ae-0b62-4eab-a07d-867b5d3d61e0": {
"match": "brand_token",
"title": "POLY-VENT DM (DEXTROMETHORPHAN HBR, GUAIFENESIN AND PSEUDOEPHEDRINE HCL) TABLET [POLY PHARMACEUTICALS, INC.]",
"spl_version": "12",
"published_date": "2025-12-22"
}
},
"productid": "50991-212_26838be8-5a59-bb4d-e063-6394a90affe9",
"productndc": "50991-212",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE",
"proprietary_name": "Poly-Vent IR",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin and Pseudoephedrine HCl",
"start_marketing_date": "20130611",
"active_numerator_strength": "380; 60"
}Related drugs
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