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United States · US · US:16103-381_fcbabd90-abc6-4a05-8841-58cb74b5a22e

PHARBINEX-DM

UNIISPLATC R05DA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerPharbest Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeR05DA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    1610338104
    1 BOTTLE, PLASTIC in 1 CARTON (16103-381-04) / 30 TABLET in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
9D2RTI9KYH
DEXTROMETHORPHAN HYDROBROMIDE
RxCUI 102490
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9D2RTI9KYH",
    "rxcui": "102490",
    "inchikey": "STTADZBLEUMJRG-IKNOHUQMSA-N",
    "display_name": "DEXTROMETHORPHAN HYDROBROMIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "8d71db43-da87-45ee-aa4a-7e870bc5016d": {
      "match": "brand_token",
      "title": "PHARBINEX-DM (GUAIFENESIN 400MG AND DEXTROMETHORPHAN HBR 20MG) TABLET [PHARBEST PHARMACEUTICALS, INC.]",
      "spl_version": "3",
      "published_date": "2025-12-26"
    }
  },
  "productid": "16103-381_fcbabd90-abc6-4a05-8841-58cb74b5a22e",
  "productndc": "16103-381",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "proprietary_name": "PHARBINEX-DM",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "GUAIFENESIN 400mg and DEXTROMETHORPHAN HBR 20MG",
  "start_marketing_date": "20180402",
  "active_numerator_strength": "20; 400"
}

Related drugs

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