Senna

UNIISPL

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

Identification

ManufacturerRite Aid Corporation

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
1182202982
1 BOTTLE, PLASTIC in 1 CARTON (11822-0298-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
ndc11
1182202984
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-0298-4)
ndc11
1182202986
1 BOTTLE, PLASTIC in 1 CARTON (11822-0298-6) / 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)

3FYP5M0IJX

SENNOSIDES

RxCUI 36387

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "3FYP5M0IJX",
    "rxcui": "36387",
    "inchikey": null,
    "display_name": "SENNOSIDES",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "491255c6-465f-a78a-e063-6394a90aa408": {
      "match": "brand_token",
      "title": "SENNA SYRUP (SENNOSIDES 8.8MG/5ML) SOLUTION [ALDAMA PHARMACEUTICALS, INC]",
      "spl_version": "2",
      "published_date": "2026-06-02"
    }
  },
  "productid": "11822-0298_a8902034-4df3-4582-a632-07b003d46a2c",
  "productndc": "11822-0298",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SENNOSIDES",
  "proprietary_name": "Senna",
  "active_ingred_unit": "mg/1",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sennosides",
  "start_marketing_date": "20241205",
  "active_numerator_strength": "8.6"
}

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