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United States · US · US:50090-6587_261e2c03-7495-4a76-aebe-8e7c795cb8e5
Ammonium Lactate
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc115009065870225 g in 1 BOTTLE, PLASTIC (50090-6587-0)
Annotations
UNII (FDA Substance ID)
67M901L9NQ
AMMONIUM LACTATE
RxCUI 215247
Orange Book
A076216
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "67M901L9NQ",
"rxcui": "215247",
"inchikey": "RZOBLYBZQXQGFY-UHFFFAOYSA-N",
"display_name": "AMMONIUM LACTATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"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": "50090-6587_261e2c03-7495-4a76-aebe-8e7c795cb8e5",
"productndc": "50090-6587",
"dosage_form": "LOTION",
"orange_book": {
"appl_no": "076216",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 12% BASE",
"product_no": "001",
"approval_date": "May 28, 2004"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "AMMONIUM LACTATE",
"proprietary_name": "Ammonium Lactate",
"active_ingred_unit": "mg/g",
"application_number": "ANDA076216",
"marketing_category": "ANDA",
"nonproprietary_name": "Ammonium Lactate",
"start_marketing_date": "20040528",
"active_numerator_strength": "120"
}Access this data programmatically
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