NDC 70518-4606
Sertraline Hydrochloride 25 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-978.
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 Lupin Pharmaceuticals, Inc. names for other drugs.
Recalls
- Nov 5, 2025 · Class II · Lupin Pharmaceuticals Inc.
Defective container - seal not adhering to bottles
Lots: Lot # QB00865, exp. date Feb 2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sertraline: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA077670
- On the market since
- Apr 22, 2026
- Package NDCs
70518-4606-070518-4606-1- Official label
- DailyMed (National Library of Medicine), updated Apr 23, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?