Ammonium Phosphoricum

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766236361
200 PELLET in 1 VIAL, GLASS (37662-3636-1)
ndc11
3766236362
500 PELLET in 1 VIAL, GLASS (37662-3636-2)
ndc11
3766236363
3000 PELLET in 1 BOTTLE, GLASS (37662-3636-3)
ndc11
3766236364
10000 PELLET in 1 BOTTLE, GLASS (37662-3636-4)

Annotations

UNII (FDA Substance ID)

10LGE70FSU

AMMONIUM PHOSPHATE, DIBASIC

RxCUI 1427061

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "10LGE70FSU",
    "rxcui": "1427061",
    "inchikey": "MNNHAPBLZZVQHP-UHFFFAOYSA-N",
    "display_name": "AMMONIUM PHOSPHATE, DIBASIC",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "030e8bd1-0ff3-479f-aa77-16fab701a111": {
      "match": "brand_token",
      "title": "AMMONIUM LACTATE CREAM [REMEDYREPACK INC.]",
      "spl_version": "5",
      "published_date": "2026-04-15"
    }
  },
  "productid": "37662-3636_00682d09-bf61-7d6f-e063-6294a90a866b",
  "productndc": "37662-3636",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMMONIUM PHOSPHATE, DIBASIC",
  "proprietary_name": "Ammonium Phosphoricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Ammonium Phosphoricum",
  "start_marketing_date": "20230713",
  "active_numerator_strength": "200"
}

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