NDC 70518-3619
Ammonium Lactate 120 mg per 1 g cream
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1301.
Where the pills inside were 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
- Jan 20, 2023
- Package NDCs
70518-3619-0- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2026
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