Tussin Long Acting Cough

UNIISPLATC N07XX59

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

Identification

ManufacturerP & L Development, LLC

CountryUS (United States)

ATC codeN07XX59

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4958003834
1 BOTTLE, PLASTIC in 1 BOX (49580-0383-4) / 118 mL 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": {
    "e1280355-da81-489f-9bd2-ffea9a68010c": {
      "match": "brand_token",
      "title": "TUSSIN COUGH AND CHEST CONGESTION DM ADULT (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [HARRIS TEETER, LLC]",
      "spl_version": "3",
      "published_date": "2026-04-30"
    }
  },
  "productid": "49580-0383_33a40dda-c597-4e8b-8195-97c527982fdd",
  "productndc": "49580-0383",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DEXTROMETHORPHAN HYDROBROMIDE",
  "proprietary_name": "Tussin Long Acting Cough",
  "active_ingred_unit": "mg/10mL",
  "application_number": "M012",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Dextromethorphan HBr",
  "start_marketing_date": "20140831",
  "active_numerator_strength": "30"
}

Related drugs

Other records sharing ATC code N07XX59.

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