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United States · US · US:58264-0347_2b52dd9d-5def-a801-e063-6294a90aeffa
AM-8
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDNA Labs, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11582640347129.57 mL in 1 BOTTLE, GLASS (58264-0347-1)
Annotations
UNII (FDA Substance ID)
WQZ3G9PF0H
ATROPA BELLADONNA
RxCUI 1363430
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WQZ3G9PF0H",
"rxcui": "1363430",
"inchikey": null,
"display_name": "ATROPA BELLADONNA",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBLINGUAL",
"spl_meta": {
"c313d3e3-11a2-45f7-8b87-1bf5d1019137": {
"match": "brand_token",
"title": "AM-8 (ATROPA BELLADONNA, CALCIUM SULFATE ANHYDROUS, AND FORMICA RUFA) SOLUTION [DNA LABS, INC.]",
"spl_version": "3",
"published_date": "2025-01-13"
}
},
"productid": "58264-0347_2b52dd9d-5def-a801-e063-6294a90aeffa",
"productndc": "58264-0347",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ATROPA BELLADONNA; CALCIUM SULFATE ANHYDROUS; FORMICA RUFA",
"proprietary_name": "AM-8",
"active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "Atropa belladonna, Calcium Sulfate Anhydrous, and Formica rufa",
"start_marketing_date": "19900101",
"active_numerator_strength": "8; 8; 12"
}Access this data programmatically
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