NDC 76420-273
Cipro Hc 2 mg per 1 mL / 10 mg per 1 mL suspension/ drops
On the label: Asclemed USA, Inc.. It's repackaged from NDC 0078-0855, made by Novartis Pharmaceuticals Corporation (Cipro). 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 relabels 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 Asclemed USA, Inc. names for other drugs.
Product details
- Generic drug
- Ciprofloxacin and Hydrocortisone: every company that makes it
- Form
- suspension/ drops, auricular (otic)
- Strength
- 2 mg per 1 mL / 10 mg per 1 mL
- Approval
- NDA NDA020805
- On the market since
- Mar 15, 1999
- Package NDCs
76420-273-10- Official label
- DailyMed (National Library of Medicine), updated Sep 7, 2022
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