NDC 68151-2482
Desipramine Hydrochloride 10 mg tablet, film coated
On the label: Carilion Materials Management. It's repackaged from NDC 0781-1971, made by Sandoz Inc (Desipramine 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 (it lists 1 site that repackages 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 Carilion Materials Management names for other drugs.
Product details
- Generic drug
- Desipramine: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA072099
- On the market since
- May 24, 1988
- Package NDCs
68151-2482-0- Official label
- DailyMed (National Library of Medicine), updated Dec 28, 2017
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