NDC 10135-643
Labetalol 300 mg tablet, film coated
On the label: Marlex Pharmaceuticals, Inc.. It's repackaged from NDC 58657-607, made by Method Pharmaceuticals, LLC (Labetalol Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
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 Marlex Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, film coated
- Strength
- 300 mg
- Approval
- ANDA ANDA075215
- On the market since
- Apr 1, 2018
- Package NDCs
10135-643-01- Official label
- DailyMed (National Library of Medicine), updated Apr 6, 2018
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