SDA Laboratories Tussin DM

UNIISPLATC R05DA

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

Identification

ManufacturerSDA Laboratories, Inc.

CountryUS (United States)

ATC codeR05DA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6642456516
473 mL in 1 BOTTLE (66424-565-16)

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": {
    "2a444cc8-96be-9432-e063-6394a90a1b63": {
      "match": "brand_token",
      "title": "SDA LABORATORIES TUSSIN (GUAIFENESIN) LIQUID [SDA LABORATORIES, INC.]",
      "spl_version": "1",
      "published_date": "2024-12-30"
    }
  },
  "productid": "66424-565_2a446fca-4094-b70a-e063-6294a90a7d2e",
  "productndc": "66424-565",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
  "proprietary_name": "SDA Laboratories Tussin DM",
  "active_ingred_unit": "mg/5mL; mg/5mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Dextromethorphan HBr, Guaifenesin",
  "start_marketing_date": "20241201",
  "active_numerator_strength": "10; 100"
}

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