Amoxicillin 125 mg per 5 mL powder, for suspension

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

• Preferred Pharmaceuticals Inc., Anaheim, CA, United States · relabels it

Recalls

• Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
  cGMP deviations: Temperature abuse
  Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
• Jan 26, 2022 · Class II · Cardinal Healthcare
  CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
  Lots: Batch LJ9004
• Apr 18, 2013 · Class II · Sandoz Incorporated
  Presence of Foreign Substance, Sandoz is recalling certain lots of Amoxicillin Capsules, USP 500 mg due to potential contamination with fragments of stainless steel wire mesh.
  Lots: CK2003, CK2004 exp. 04/15, CR4110, CR4111, CS2983, CS2986, CS2988, CS2989, CS2990, CS2991, CS2992, CS2993, CS2994 exp. 07/15, CK3616, CK3617 exp. 04/15

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: every company that makes it

Form

powder, for suspension, oral

Strength

125 mg per 5 mL

Approval

ANDA ANDA065387

On the market since

Jan 12, 2012

Package NDCs

68788-9949-1

Official label

DailyMed (National Library of Medicine), updated Jan 26, 2026

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