Senna

UNIISPL

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7133523601
100 TABLET in 1 BOTTLE (71335-2360-1)
ndc11
7133523602
60 TABLET in 1 BOTTLE (71335-2360-2)
ndc11
7133523603
120 TABLET in 1 BOTTLE (71335-2360-3)
ndc11
7133523604
56 TABLET in 1 BOTTLE (71335-2360-4)
ndc11
7133523605
30 TABLET in 1 BOTTLE (71335-2360-5)
ndc11
7133523606
90 TABLET in 1 BOTTLE (71335-2360-6)
ndc11
7133523607
10 TABLET in 1 BOTTLE (71335-2360-7)

Annotations

UNII (FDA Substance ID)

1B5FPI42EN

SENNOSIDES A AND B

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1B5FPI42EN",
    "rxcui": null,
    "inchikey": null,
    "display_name": "SENNOSIDES A AND B",
    "substance_type": "mixture",
    "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": "71335-2360_e9ee7425-5a71-4b17-abd2-3df62474549f",
  "productndc": "71335-2360",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SENNOSIDES A AND B",
  "proprietary_name": "Senna",
  "active_ingred_unit": "mg/1",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sennosides",
  "start_marketing_date": "20200801",
  "active_numerator_strength": "8.6"
}

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