NDC 53002-3451
Dicyclomine Hydrochloride 20 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, 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
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Dicyclomine: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA040230
- On the market since
- Feb 26, 1999
- Package NDCs
53002-3451-153002-3451-253002-3451-353002-3451-4- Official label
- DailyMed (National Library of Medicine), updated Jan 31, 2023
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