NDC 54868-4560
Fluoxetine Hydrochloride 10 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 49884-734, made by Par Pharmaceutical, Inc (Fluoxetine Hydrochloride). 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA075755
- On the market since
- Aug 19, 2003
- Package NDCs
54868-4560-054868-4560-154868-4560-2- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2009
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