NDC 42852-001
Ciprofloxacin Hydrochloride 500 mg tablet
On the label: Apothecary Shop Wholesale Inc.. It's repackaged from NDC 55111-127, made by Dr. Reddy's Laboratories Limited (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 Apothecary Shop Wholesale Inc. names for other drugs.
Recalls
- May 3, 2019 · Class II · Avella of Deer Valley, Inc. Store 38
Lack of assurance of sterility
Lots: Lot #: 138-20191202@64, Exp 05/13/19 - Oct 31, 2018 · Class II · Avella of Deer Valley, Inc. Store 38
Lack of Assurance of Sterility
Lots: Lot # 138-20182408@58 BUD 12/22/2018
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
- tablet
- Strength
- 500 mg
- Approval
- ANDA ANDA075593
- On the market since
- Jul 1, 2011
- Package NDCs
42852-001-02- Official label
- DailyMed (National Library of Medicine), updated Jun 21, 2011
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