NDC 68387-550
Mupirocin 20 mg per 1 g ointment
On the label: Keltman Pharmaceuticals Inc.. It's repackaged from NDC 0168-0352, made by E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. (Mupirocin). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Keltman Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Mupirocin: every company that makes it
- Form
- ointment
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA065192
- On the market since
- Jun 22, 2009
- Package NDCs
68387-550-01- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2011
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