NDC 51672-1310

Betamethasone Dipropionate 0.5 mg per 1 g cream, augmented

On the label: Caraco Pharmaceutical Laboratories, Ltd..

Canada: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Sun Pharma Canada Inc.Brampton, CanadaMakes it No problems foundMar 27, 2026 · 7 inspections

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
51672-1310-1 51672-1310-2 51672-1310-3
Official label
DailyMed (National Library of Medicine), updated Sep 26, 2025

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