NDC 66116-607
Cephalexin 250 mg per 5 mL powder, for suspension
On the label: MedVantx, Inc.. It's repackaged: MedVantx, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-4177.
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
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it
Recalls
- Aug 24, 2020 · Class II · Teva Pharmaceuticals USA
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Lots: Lot #s: a) 30309862A, 30309863A, Exp. 08/2020; 30309928A, 30309929A, Exp. 09/2020; 30310029A, 30310030A, 30310033A, 30310034A, Exp. 10/2020; 30310035A, 30310079A, 30310080A, 30310081A, Exp. 11/2020; 30310134A, 30310135A, Exp. 01/2021; 30310182A, 30310183A, 30310210A, Exp. 02/2021; 30310211A, 30… - Aug 24, 2020 · Class II · Teva Pharmaceuticals USA
Sub-Potent Drug: Out of specification test results for potency (below specification).
Lots: Lot #: 30310638A, Exp. 02/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cephalexin: every company that makes it
- Form
- powder, for suspension
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA062703
- On the market since
- Sep 30, 1990
- Package NDCs
66116-607-20- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2012
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