NDC 70518-4624
Neomycin Sulfate 500 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-1177.
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.
Recalls
- Aug 23, 2022 · Class II · Teva Pharmaceuticals USA Inc
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Lots: Lot #: 3007830, 3007746, 3007829, Exp. Date 10/2024 - Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 3006910
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Neomycin: every company that makes it
- Form
- tablet, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA060304
- On the market since
- Apr 24, 2026
- Package NDCs
70518-4624-070518-4624-1- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2026
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