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United States Β· US Β· US:37662-3609_0053de7d-eeef-5489-e063-6294a90a0514
Ammonium Carbonicum
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 3
- ndc113766236091200 PELLET in 1 VIAL, GLASS (37662-3609-1)
- ndc1137662360921200 PELLET in 1 BOTTLE, GLASS (37662-3609-2)
- ndc1137662360934000 PELLET in 1 BOTTLE, GLASS (37662-3609-3)
Annotations
UNII (FDA Substance ID)
NJ5VT0FKLJ
AMMONIUM CARBONATE
RxCUI 1310190
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "NJ5VT0FKLJ",
"rxcui": "1310190",
"inchikey": null,
"display_name": "AMMONIUM CARBONATE",
"substance_type": "mixture",
"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": "37662-3609_0053de7d-eeef-5489-e063-6294a90a0514",
"productndc": "37662-3609",
"dosage_form": "PELLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AMMONIUM CARBONATE",
"proprietary_name": "Ammonium Carbonicum",
"active_ingred_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Ammonium Carbonicum",
"start_marketing_date": "20230712",
"active_numerator_strength": "12"
}Access this data programmatically
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