NDC 70934-250
Atorvastatin Calcium 10 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Apotex Corp.'s NDC 60505-2578.
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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages 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
- 10 mg
- Approval
- ANDA ANDA090548
- On the market since
- Jan 21, 2019
- Package NDCs
70934-250-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?