NDC 54868-6178
Paroxetine Hydrochloride 12.5 mg tablet, film coated, extended release
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0378-2003, made by Mylan Pharmaceuticals Inc. (Paroxetine 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
- Paroxetine: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 12.5 mg
- Approval
- ANDA ANDA077873
- On the market since
- Oct 25, 2010
- Package NDCs
54868-6178-0- Official label
- DailyMed (National Library of Medicine), updated May 17, 2011
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