NDC 51672-1301
Ammonium Lactate 120 mg per 1 g cream
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Product details
- Generic drug
- Lactic Acid, Unspecified Form: every company that makes it
- Form
- cream, topical
- Strength
- 120 mg per 1 g
- Approval
- ANDA ANDA075883
- On the market since
- Apr 10, 2003
- Package NDCs
51672-1301-051672-1301-251672-1301-4- Official label
- DailyMed (National Library of Medicine), updated Aug 17, 2026
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