NDC 68682-271
Hydrocortisone Butyrate 1 mg per 1 g ointment
On the label: Oceanside Pharmaceuticals..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ferndale Laboratories, Inc. | Ferndale, MI, United States | Makes it | Problems found, fixed voluntarilyFeb 27, 2026 · 10 inspections, 2 with FDA action |
Product details
- Generic drug
- Hydrocortisone: every company that makes it
- Form
- ointment, topical
- Strength
- 1 mg per 1 g
- Approval
- NDA NDA018652
- On the market since
- Sep 1, 2009
- Package NDCs
68682-271-1568682-271-45- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2020
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