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United States · US · US:71335-9616_97d545be-a78d-48b5-b774-ded0e82d742f
Guaifenesin
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11713359616130 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)
- ndc11713359616220 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2)
- ndc11713359616350 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3)
- ndc11713359616460 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4)
- ndc11713359616540 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)
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": {
"9cfb1abb-98c4-4e90-8dd7-fcffc112f988": {
"match": "brand_token",
"title": "GUAIFENESIN DM (GUAIFENESIN AND DEXTROMETHORPHAN) SYRUP [CARDINAL HEALTH 107, LLC]",
"spl_version": "8",
"published_date": "2026-05-21"
}
},
"productid": "71335-9616_97d545be-a78d-48b5-b774-ded0e82d742f",
"productndc": "71335-9616",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Guaifenesin",
"active_ingred_unit": "mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20200801",
"active_numerator_strength": "400"
}Related drugs
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