ammonium lactate
Generic: ammonium lactate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
ammonium lactate
Generic Name
ammonium lactate
Labeler
a-s medication solutions
Dosage Form
LOTION
Routes
Active Ingredients
ammonium lactate 120 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6587
Product ID
50090-6587_261e2c03-7495-4a76-aebe-8e7c795cb8e5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076216
Listing Expiration
2026-12-31
Marketing Start
2004-05-28
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906587
Hyphenated Format
50090-6587
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ammonium lactate (source: ndc)
Generic Name
ammonium lactate (source: ndc)
Application Number
ANDA076216 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 120 mg/g
Packaging
- 225 g in 1 BOTTLE, PLASTIC (50090-6587-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "261e2c03-7495-4a76-aebe-8e7c795cb8e5", "openfda": {"nui": ["N0000175842", "M0010745"], "unii": ["67M901L9NQ"], "rxcui": ["197362"], "spl_set_id": ["ab54704d-ace2-410c-b0af-2fa13462a8b3"], "pharm_class_cs": ["Hydroxy Acids [CS]"], "pharm_class_epc": ["alpha-Hydroxy Acid [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "225 g in 1 BOTTLE, PLASTIC (50090-6587-0)", "package_ndc": "50090-6587-0", "marketing_start_date": "20230810"}], "brand_name": "Ammonium Lactate", "product_id": "50090-6587_261e2c03-7495-4a76-aebe-8e7c795cb8e5", "dosage_form": "LOTION", "pharm_class": ["Acidifying Activity [MoA]"], "product_ndc": "50090-6587", "generic_name": "Ammonium Lactate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ammonium Lactate", "active_ingredients": [{"name": "AMMONIUM LACTATE", "strength": "120 mg/g"}], "application_number": "ANDA076216", "marketing_category": "ANDA", "marketing_start_date": "20040528", "listing_expiration_date": "20261231"}