robafen dm

UNIISPLATC R05DA

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerPreferred Pharmaceuticals Inc.

CountryUS (United States)

ATC codeR05DA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6878882681
1 BOTTLE in 1 CARTON (68788-8268-1) / 118 mL in 1 BOTTLE

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": {
    "5e19220d-9cf3-4732-b9aa-c09db5d69ce6": {
      "match": "brand_token",
      "title": "ROBAFEN DM (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN) SOLUTION [MAJOR PHARMACEUTICALS]",
      "spl_version": "4",
      "published_date": "2026-03-03"
    }
  },
  "productid": "68788-8268_95130e72-3bba-4927-b4fb-1f4f3cd8f65d",
  "productndc": "68788-8268",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "proprietary_name": "robafen dm",
  "active_ingred_unit": "mg/20mL; mg/20mL",
  "application_number": "part341",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "dextromethorphan hydrobromide, guaifenesin",
  "start_marketing_date": "20220923",
  "active_numerator_strength": "20; 200"
}

Related drugs

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