NDC 21695-449
Mefloquine Hydrochloride 250 mg tablet
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-0171.
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.
Recalls
- Apr 2, 2012 · Class II · Teva Pharmaceuticals USA, Inc.
Tablet Thickness: Product is being recalled due to the potential of being underweight or overweight.
Lots: Lot # 34000741A; Expiration date: 7/2013
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Mefloquine: every company that makes it
- Form
- tablet
- Strength
- 250 mg
- Approval
- ANDA ANDA076392
- On the market since
- Dec 29, 2003
- Package NDCs
21695-449-0721695-449-25- Official label
- DailyMed (National Library of Medicine), updated Dec 28, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?