NDC 68071-4556
Betamethasone Dipropionate 0.5 mg per 1 g cream, augmented
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1310.
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 |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Betamethasone: every company that makes it
- Form
- cream, augmented, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA076543
- On the market since
- Dec 9, 2003
- Package NDCs
68071-4556-368071-4556-5- Official label
- DailyMed (National Library of Medicine), updated Apr 3, 2025
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