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United States · US · US:0485-0208_423e6598-ff90-d9d4-e063-6294a90a1fba
ED BRON GP
UNIISPLATC R05CA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEDWARDS PHARMACEUTICALS, INC.
CountryUS (United States)
ATC codeR05CA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110485020816473 mL in 1 BOTTLE, PLASTIC (0485-0208-16)
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": {
"e0e2b117-62bc-4132-9f7c-fe2a912052b1": {
"match": "brand_token",
"title": "ED A-HIST DM (DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE HYDROCHLORIDE) LIQUID [EDWARDS PHARMACEUTICALS, INC.]",
"spl_version": "10",
"published_date": "2026-01-01"
}
},
"productid": "0485-0208_423e6598-ff90-d9d4-e063-6294a90a1fba",
"productndc": "0485-0208",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
"proprietary_name": "ED BRON GP",
"active_ingred_unit": "mg/5mL; mg/5mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "GUAIFENESIN and PHENYLEPHRINE",
"start_marketing_date": "20120601",
"active_numerator_strength": "100; 5"
}Related drugs
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