United States · FDA National Drug Code directory
Ammonium Lactate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51672-1300_57d7e3ba-2c3e-a79b-e063-6394a90a4a5b
- Product NDC
- 51672-1300
- Form
- LOTION
- Composition / generic term
- Ammonium Lactate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040528
- Source listing expiry
- 20271231
Source-listed ingredients
- AMMONIUM LACTATE — 120 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 225 g in 1 BOTTLE, PLASTIC (51672-1300-5) · 51672-1300-5
- 400 g in 1 BOTTLE, PLASTIC (51672-1300-9) · 51672-1300-9
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →