NDC 0143-9887
Amoxicillin 400 mg per 5 mL powder, for suspension
On the label: Hikma Pharmaceuticals USA Inc..
Where it's 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.
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
- Jun 19, 2006
- Package NDCs
0143-9887-010143-9887-500143-9887-75- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2024
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