NDC 11819-323
Ciprofloxacin 500 mg tablet, film coated
On the label: HHS/Program Support Center/Supply Service Center. It's repackaged: HHS/Program Support Center/Supply Service Center rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 16252-515.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA076794
- On the market since
- Jun 9, 2004
- Package NDCs
11819-323-30- Official label
- DailyMed (National Library of Medicine), updated Jan 3, 2012
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