NDC 68071-4302
Atorvastatin Calcium 20 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Apotex Corp.'s NDC 60505-2579.
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 Apotex Corp. names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Oct 22, 2019 · Class III · Apotex Inc.
Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg found in bottle of Atorvastatin Calcium 40 mg.
Lots: Lot: RC5439 Exp. 03/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Atorvastatin: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA090548
- On the market since
- May 29, 2012
- Package NDCs
68071-4302-9- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2021
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