NDC 70518-2871
Paroxetine 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Apotex Corp.'s NDC 60505-0083.
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: a)100 count bottle: RV2384, RV2385; b) 1000 count bottle: RV2396, RV2397; 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, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075356
- On the market since
- Sep 8, 2020
- Package NDCs
70518-2871-070518-2871-1- Official label
- DailyMed (National Library of Medicine), updated Sep 28, 2026
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