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
70518-3619_4f6bc7a2-ebb4-9e33-e063-6294a90a394e
Product NDC
70518-3619
Form
CREAM
Composition / generic term
Ammonium Lactate
Labeler
REMEDYREPACK INC.
Marketing category
ANDA
Marketing start / end (source format)
20230120
Source listing expiry
20271231

Source-listed ingredients

  • AMMONIUM LACTATE — 120 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 TUBE in 1 CARTON (70518-3619-0) / 140 g in 1 TUBE · 70518-3619-0

Source and coverage

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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.

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