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United States · US · US:68163-743_3fef020a-9ccf-8f8a-e063-6394a90a376e
DRx Choice
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRaritan Pharmaceuticals Inc
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1168163743041 BOTTLE in 1 CARTON (68163-743-04) / 118 mL 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": {
"f466fc0e-3384-4884-832e-99bf1fdcf899": {
"match": "brand_token",
"title": "DRX CHOICE NIGHTTIME COLD AND FLU RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE) CAPSULE, LIQUID FILLED [RARITAN PHARMACEUTICALS INC.]",
"spl_version": "1",
"published_date": "2026-01-23"
}
},
"productid": "68163-743_3fef020a-9ccf-8f8a-e063-6394a90a376e",
"productndc": "68163-743",
"dosage_form": "SYRUP",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "DRx Choice",
"active_ingred_unit": "mg/10mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20190515",
"active_numerator_strength": "200"
}Related drugs
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