NDC 21695-277
Lyrica 50 mg capsule
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Parke-Davis Div of Pfizer Inc's NDC 0071-1013.
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 Parke-Davis Div of Pfizer Inc names for other drugs.
Recalls
- Jan 11, 2016 · Class II · Pfizer Inc.
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Lots: Lot #: M07861, Exp 05/2018 - Jan 11, 2016 · Class II · Pfizer Inc.
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Lots: Lot #: M07862, Exp 05/2018; M07865, Exp 06/2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pregabalin: every company that makes it
- Form
- capsule
- Strength
- 50 mg
- Approval
- NDA NDA021724
- On the market since
- Jun 10, 2005
- Package NDCs
21695-277-1521695-277-3021695-277-90- 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?