NDC 68071-2868
Dicyclomine Hydrochloride 20 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- NuCare Pharmaceuticals,Inc., Orange, CA, 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
- Feb 26, 1999
- Package NDCs
68071-2868-6- Official label
- DailyMed (National Library of Medicine), updated Nov 3, 2022
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