NDC 51672-1340
Betamethasone Dipropionate 0.5 mg per 1 mL lotion, augmented
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
- Betamethasone: every company that makes it
- Form
- lotion, augmented, topical
- Strength
- 0.5 mg per 1 mL
- Approval
- ANDA ANDA077477
- On the market since
- May 21, 2007
- Package NDCs
51672-1340-351672-1340-4- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2025
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