NDC 53808-0236
Didanosine 250 mg capsule, delayed release pellets
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 0555-0589, made by Teva Pharmaceuticals USA, Inc. (Didanosine). 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Didanosine: every company that makes it
- Form
- capsule, delayed release pellets
- Strength
- 250 mg
- Approval
- ANDA ANDA077167
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0236-1- Official label
- DailyMed (National Library of Medicine), updated Aug 11, 2010
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