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United States · US · US:69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c

Somnapure

UNIISPLATC D04AA32

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

Identification

ManufacturerForce Factor Brands LLC
CountryUS (United States)
ATC codeD04AA32
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6972100530
    1 BOTTLE in 1 CARTON (69721-005-30) / 30 TABLET, COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
TC2D6JAD40
DIPHENHYDRAMINE HYDROCHLORIDE
RxCUI 1362
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "TC2D6JAD40",
    "rxcui": "1362",
    "inchikey": "PCHPORCSPXIHLZ-UHFFFAOYSA-N",
    "display_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "063517c0-bcb1-46dd-85f1-bbb2f24274ef": {
      "match": "brand_token",
      "title": "SOMNAPURE CLINICAL STRENGTH (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, COATED [FORCE FACTOR BRANDS LLC]",
      "spl_version": "4",
      "published_date": "2024-12-10"
    }
  },
  "productid": "69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c",
  "productndc": "69721-005",
  "dosage_form": "TABLET, COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DIPHENHYDRAMINE HYDROCHLORIDE",
  "proprietary_name": "Somnapure",
  "active_ingred_unit": "mg/1",
  "application_number": "M010",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Diphenhydramine Hydrochloride",
  "start_marketing_date": "20180320",
  "active_numerator_strength": "50"
}

Related drugs

Other records sharing ATC code D04AA32.

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