NDC 70518-3624
Amoxicillin and Clavulanate Potassium 125 mg / 875 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Sandoz Inc.'s NDC 0781-1852.
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 Sandoz Inc. names for other drugs.
Recalls
- Apr 26, 2017 · Class III · Sandoz Inc
Subpotent Drug; Clavulanic Acid
Lots: Lot FP8735, 8/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Amoxicillin and Clavulanic Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 125 mg / 875 mg
- Approval
- ANDA ANDA065063
- On the market since
- Jan 27, 2023
- Package NDCs
70518-3624-070518-3624-170518-3624-270518-3624-370518-3624-470518-3624-5- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?