NDC 63739-112
Furosemide 40 mg tablet
On the label: McKesson Packaging Services Business Unit of McKesson Corporation. It's repackaged from NDC 0781-1966, made by Sandoz Inc (Furosemide). 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 McKesson Packaging Services Business Unit of McKesson Corporation names for other drugs.
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA018569
- On the market since
- Oct 1, 2004
- Package NDCs
63739-112-0163739-112-0363739-112-10- Official label
- DailyMed (National Library of Medicine), updated Jun 13, 2011
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