NDC 72189-104
Desipramine Hydrochloride 10 mg tablet, film coated
On the label: Direct Rx. It's repackaged from NDC 0781-8218, 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 Direct Rx 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
- Jun 12, 2020
- Package NDCs
72189-104-30- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?