NDC 67296-0543
Ciprofloxacin Hydrochloride 500 mg tablet
On the label: RedPharm Drug Inc.. It's repackaged from NDC 0172-5312, made by Teva Pharmaceuticals USA, Inc. (Ciprofloxacin). 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 RedPharm Drug Inc. names for other drugs.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet
- Strength
- 500 mg
- Approval
- ANDA ANDA076089
- On the market since
- Apr 4, 2011
- Package NDCs
67296-0543-267296-0543-367296-0543-467296-0543-5- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2011
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