NDC 51672-1301 – Ammonium Lactate

Ammonium Lactate 120 mg/g · Cream · Topical

Human Prescription Drug

Product NDC51672-1301

Product details

Brand name
Ammonium Lactate
Generic name
Ammonium Lactate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA075883
Marketed since
April 10, 2003
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Ammonium Lactate →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1301-0385 g in 1 BOTTLE, PLASTIC (51672-1301-0)Apr 10, 2003
51672-1301-21 TUBE in 1 CARTON (51672-1301-2) / 140 g in 1 TUBEJul 1, 2024
51672-1301-42 TUBE in 1 CARTON (51672-1301-4) / 140 g in 1 TUBEApr 10, 2003

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