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United States · US · US:73564-801_51db82e3-4f0c-1d08-e063-6394a90aae3d
Guaifed
UNIISPLATC R05CA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAldama Pharmaceuticals, Inc
CountryUS (United States)
ATC codeR05CA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc117356480104118 mL in 1 BOTTLE (73564-801-04)
- ndc117356480108237 mL in 1 BOTTLE (73564-801-08)
- ndc117356480116473 mL in 1 BOTTLE (73564-801-16)
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": {
"396bf716-0f61-9563-e063-6394a90a171b": {
"match": "brand_token",
"title": "GUAIFED DM (DEXTROMETHORPHAN, GUAIFENESIN) LIQUID [ALDAMA PHARMACEUTICALS, INC]",
"spl_version": "5",
"published_date": "2026-06-02"
}
},
"productid": "73564-801_51db82e3-4f0c-1d08-e063-6394a90aae3d",
"productndc": "73564-801",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "GUAIFENESIN",
"proprietary_name": "Guaifed",
"active_ingred_unit": "mg/10mL",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Guaifenesin",
"start_marketing_date": "20260601",
"active_numerator_strength": "200"
}Related drugs
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