NDC 61919-095
Baclofen 20 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Lannett Company, Inc.'s NDC 0527-1337.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Product details
- Generic drug
- Baclofen: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077241
- On the market since
- Jan 1, 2014
- Package NDCs
61919-095-6061919-095-8261919-095-90- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?