NDC 53808-0754
paroxetine 40 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Apotex Corp.'s NDC 60505-0101.
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 Apotex Corp. names for other drugs.
Recalls
- Nov 1, 2023 · Class II · Apotex Corp.
Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine
Lots: Lot numbers: RV0131, RV2387, RV2389, RW3296, RV2388; Exp. 08/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Paroxetine: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA075356
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0754-1- Official label
- DailyMed (National Library of Medicine), updated May 29, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?