NDC 42708-112

Amoxicillin 875 mg tablet, film coated

On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-2264.

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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch 35447184A
Jun 24, 2016 · Class II · Teva North America
Superpotent drug: Out of specification test result for assay during stability testing.
Lots: Lot # 35434158A, Exp 6/17
Jun 18, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Discoloration: This recall is being carried out due to an orange to brown discolored Amoxicillin powder on the inner foil seal of the bottles. This is an expansion of RES 65050.
Lots: Lot #s: a) 35426557A, 35426558A, Exp 08/14; b) 35426554A, 35426555A, 35426556A, Exp 08/14
Apr 26, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Discoloration: This recall is being carried out due to a yellow to brown discolored Amoxicillin powder on the inner foil seal of the bottles.
Lots: a) NDC 0093-4161-78 -- lot numbers 35426081A, 35426082A, 35426083A, 35426084A, Exp: 06/2014; 35426648A, Exp 08/2014; 35427222A, 35427224A, 35427226A, 35427223A, 35427227A, 35427228A, Exp 10/2014; and b) NDC 0093-4161-73 -- lot numbers 35426631A, 35426632A, 35426633A, 35426634A, 35426635A, 3542663…

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Generic drug: Amoxicillin: every company that makes it
Form: tablet, film coated, oral
Strength: 875 mg
Approval: ANDA ANDA065056
On the market since: Sep 26, 2000
Package NDCs: 42708-112-20
Official label: DailyMed (National Library of Medicine), updated Dec 19, 2025

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