NDC 44523-550
Sodium Sulfacetamide, Sulfur 20 mg per 1 g / 100 mg per 1 g emulsion
On the label: Biocomp Pharma, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Medical Products Laboratories, Inc. | Philadelphia, PA, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 13, 2023 · 8 inspections |
Product details
- Generic drug
- Sulfacetamide and Sulfur: every company that makes it
- Form
- emulsion, topical
- Strength
- 20 mg per 1 g / 100 mg per 1 g
- Approval
- unapproved drug other
- On the market since
- Sep 15, 2011
- Package NDCs
44523-550-08- Official label
- DailyMed (National Library of Medicine), updated Aug 24, 2023
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