NDC 68071-3035
Dicyclomine Hydrochloride 10 mg capsule
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Lannett Company, Inc.'s NDC 0527-0586.
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
- capsule, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA084285
- On the market since
- Sep 30, 1974
- Package NDCs
68071-3035-3- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2024
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