NDC 72189-385
Amoxil 400 mg per 5 mL powder, for suspension
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9887.
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 Hikma Pharmaceuticals USA Inc. names for other drugs.
Repackaging site
- Direct Rx, Dawsonville, GA, United States · relabels it
Recalls
- Nov 4, 2016 · Class III · West-Ward Pharmaceuticals Corp.
Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
Lots: Lot #: AS1466A, Exp. Jan 2019
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
- 400 mg per 5 mL
- Approval
- ANDA ANDA065325
- On the market since
- Oct 21, 2022
- Package NDCs
72189-385-32- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?