Emetrol Powder

UNIISPLATC A09AB

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

Identification

ManufacturerWellSpring Pharmaceutical Corporation

CountryUS (United States)

ATC codeA09AB

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6519720309
6 POWDER, FOR SOLUTION in 1 CARTON (65197-203-09)

Annotations

UNII (FDA Substance ID)

B22547B95K

TRISODIUM CITRATE DIHYDRATE

RxCUI 221163

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "B22547B95K",
    "rxcui": "221163",
    "inchikey": "NLJMYIDDQXHKNR-UHFFFAOYSA-K",
    "display_name": "TRISODIUM CITRATE DIHYDRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9880a18a-cf84-47cd-99b5-d692065a25bf": {
      "match": "brand_token",
      "title": "EMETROL CHEWABLES (SODIUM CITRATE DIHYDRATE) TABLET, CHEWABLE [WELLSPRING PHARMACEUTICAL CORPORATION]",
      "spl_version": "7",
      "published_date": "2025-11-21"
    }
  },
  "productid": "65197-203_a6121b17-e850-4677-9ad1-ceb36de16336",
  "productndc": "65197-203",
  "dosage_form": "POWDER, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TRISODIUM CITRATE DIHYDRATE",
  "proprietary_name": "Emetrol Powder",
  "active_ingred_unit": "mg/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER",
  "nonproprietary_name": "Sodium Citrate Dihydrate",
  "start_marketing_date": "20231201",
  "active_numerator_strength": "460"
}

Related drugs

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