NDC 76420-858

Betamethasone Dipropionate 0.5 mg per 1 g cream, augmented

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1310.

Canada: 1

Where the pills inside were made

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

Repackaging site

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
76420-858-15 76420-858-30 76420-858-50
Official label
DailyMed (National Library of Medicine), updated Oct 11, 2024

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