NDC 33261-910
Ciprofloxacin Hydrochloride 3 mg per 1 mL solution/ drops
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Sandoz Inc.'s NDC 61314-656.
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 Sandoz Inc. names for other drugs.
Repackaging site
- Aidarex Pharmaceuticals, Location not on file · relabels it
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- solution/ drops
- Strength
- 3 mg per 1 mL
- Approval
- NDA AUTHORIZED GENERIC NDA019992
- On the market since
- Apr 3, 2018
- Package NDCs
33261-910-01- Official label
- DailyMed (National Library of Medicine), updated Aug 21, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?