NDC 68071-2853
Amoxicillin and Clavulanate Potassium 125 mg / 875 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.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.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
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
- Strength
- 125 mg / 875 mg
- Approval
- ANDA ANDA065063
- On the market since
- Mar 14, 2002
- Package NDCs
68071-2853-2- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2022
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