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United States · US · US:58980-913_119ef16e-c873-41df-9e98-4ccade286a85

Peviderm Pramoxine Hydrocholride 1%

UNIISPLATC D04AB07

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

Identification

ManufacturerStratus Pharmaceuticals Inc
CountryUS (United States)
ATC codeD04AB07
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5898091380
    1 BOTTLE in 1 BOX (58980-913-80) / 222 mL in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
88AYB867L5
PRAMOXINE HYDROCHLORIDE
RxCUI 57555
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "88AYB867L5",
    "rxcui": "57555",
    "inchikey": "SYCBXBCPLUFJID-UHFFFAOYSA-N",
    "display_name": "PRAMOXINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "680b40fa-1922-443a-a4b0-7c3f6a2b847d": {
      "match": "brand_token",
      "title": "PEVIDERM PRAMOXINE HYDROCHOLRIDE 1% (PRAMOXINE HYDROCHLORIDE) LOTION [STRATUS PHARMACEUTICALS INC]",
      "spl_version": "2",
      "published_date": "2024-11-11"
    }
  },
  "productid": "58980-913_119ef16e-c873-41df-9e98-4ccade286a85",
  "productndc": "58980-913",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PRAMOXINE HYDROCHLORIDE",
  "proprietary_name": "Peviderm Pramoxine Hydrocholride 1%",
  "active_ingred_unit": "mg/mL",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Pramoxine Hydrochloride",
  "start_marketing_date": "20241101",
  "active_numerator_strength": "1"
}

Related drugs

Other records sharing ATC code D04AB07.

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