NDC 51672-4061

Hydrocortisone Butyrate 1 mg per 1 mL solution

On the label: Caraco Pharmaceutical Laboratories, Ltd..

Israel: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Taro Pharmaceutical Industries Ltd.Haifa Bay, IsraelMakes it No problems foundDec 8, 2022 · 7 inspections

Product details

Generic drug
Hydrocortisone: every company that makes it
Form
solution, topical
Strength
1 mg per 1 mL
Approval
ANDA ANDA076364
On the market since
Jan 14, 2004
Package NDCs
51672-4061-2 51672-4061-4
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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