NDC 67296-1053
Terbutaline Sulfate 2.5 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-1318.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Terbutaline: every company that makes it
- Form
- tablet
- Strength
- 2.5 mg
- Approval
- ANDA ANDA077152
- On the market since
- Mar 25, 2005
- Package NDCs
67296-1053-6- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2022
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