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United States · US · US:51672-1301_38e5b035-6ea3-605e-e063-6294a90a7087
Ammonium Lactate
Orange BookUNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc115167213010385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
- ndc1151672130121 TUBE in 1 CARTON (51672-1301-2) / 140 g in 1 TUBE
- ndc1151672130142 TUBE in 1 CARTON (51672-1301-4) / 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": "51672-1301_38e5b035-6ea3-605e-e063-6294a90a7087",
"productndc": "51672-1301",
"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": "20030410",
"active_numerator_strength": "120"
}Access this data programmatically
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