NDC 63739-192
Phenobarbital 16.2 mg tablet
On the label: McKesson Packaging Services Business Unit of McKesson Corporation. It's repackaged from NDC 13517-110, made by e5 Pharma, LLC (Phenobarbital). 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 (it lists 1 site that repackages it and relabels it). 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 McKesson Packaging Services Business Unit of McKesson Corporation names for other drugs.
Product details
- Generic drug
- Phenobarbital: every company that makes it
- Form
- tablet
- Strength
- 16.2 mg
- Approval
- unapproved drug other
- On the market since
- Feb 24, 2017
- Package NDCs
63739-192-10- Official label
- DailyMed (National Library of Medicine), updated Mar 5, 2025
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