NDC 10544-560
Dicyclomine Hydrochloride 20 mg tablet
On the label: Blenheim Pharmacal, Inc.. It's repackaged: Blenheim Pharmacal, Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-1282.
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
- Blenheim Pharmacal, Inc., North Blenheim, New York, United States · repackages it
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA040230
- On the market since
- Nov 13, 2013
- Package NDCs
10544-560-3010544-560-90- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2015
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