Ammonium Lactate 51672-1301
Product NDC
51672-1301- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- April 10, 2003
- Listing Expires
- December 31, 2026
- Application
- ANDA075883
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ammonium Lactate | 120 mg/g |
Drug Class
alpha-Hydroxy Acid [EPC]Acidifying Activity [MoA]
Packaging Options(3)
385 g in 1 BOTTLE, PLASTIC (51672-1301-0)
1 TUBE in 1 CARTON (51672-1301-2) / 140 g in 1 TUBE
2 TUBE in 1 CARTON (51672-1301-4) / 140 g in 1 TUBE