Ammonium Bromatum

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
3766236041
200 PELLET in 1 VIAL, GLASS (37662-3604-1)
ndc11
3766236042
500 PELLET in 1 VIAL, GLASS (37662-3604-2)
ndc11
3766236043
3000 PELLET in 1 BOTTLE, GLASS (37662-3604-3)
ndc11
3766236044
10000 PELLET in 1 BOTTLE, GLASS (37662-3604-4)

Annotations

UNII (FDA Substance ID)

R0JB3224WS

AMMONIUM BROMIDE

RxCUI 1313309

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "R0JB3224WS",
    "rxcui": "1313309",
    "inchikey": "SWLVFNYSXGMGBS-UHFFFAOYSA-N",
    "display_name": "AMMONIUM BROMIDE",
    "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": "37662-3604_00537772-4bd0-36ee-e063-6294a90a3d66",
  "productndc": "37662-3604",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMMONIUM BROMIDE",
  "proprietary_name": "Ammonium Bromatum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Ammonium Bromatum",
  "start_marketing_date": "20230712",
  "active_numerator_strength": "200"
}

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