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United States · US · US:70518-3619_4f6bc7a2-ebb4-9e33-e063-6294a90a394e
Ammonium Lactate
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170518361902 TUBE in 1 CARTON (70518-3619-0) / 140 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
67M901L9NQ
AMMONIUM LACTATE
RxCUI 215247
Orange Book
A075883
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": "70518-3619_4f6bc7a2-ebb4-9e33-e063-6294a90a394e",
"productndc": "70518-3619",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "075883",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "EQ 12% BASE",
"product_no": "001",
"approval_date": "Apr 10, 2003"
}
],
"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": "ANDA075883",
"marketing_category": "ANDA",
"nonproprietary_name": "Ammonium Lactate",
"start_marketing_date": "20230120",
"active_numerator_strength": "120"
}Access this data programmatically
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