NDC 63629-8812
Fluvastatin 20 mg capsule
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7442.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- May 29, 2014 · Class II · Teva Pharmaceuticals USA
Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Fluvastatin Capsules USP, 20 mg due to a customer complaint trend regarding capsule breakage.
Lots: Lot #: F47008, Exp. 7/2015
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluvastatin: every company that makes it
- Form
- capsule, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078407
- On the market since
- Jul 5, 2012
- Package NDCs
63629-8812-1- Official label
- DailyMed (National Library of Medicine), updated Jan 11, 2024
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