NDC 52959-739
Ciprofloxacin 250 mg tablet, film coated
On the label: H.J. Harkins Co., Inc.. It's repackaged: H.J. Harkins Co., Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 16252-514.
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
- 250 mg
- Approval
- ANDA ANDA076794
- On the market since
- Jun 9, 2004
- Package NDCs
52959-739-0652959-739-1452959-739-2052959-739-30- Official label
- DailyMed (National Library of Medicine), updated Nov 30, 2011
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