NDC 61919-904
Dicyclomine Hydrochloride 20 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, 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
- Mar 14, 2018
- Package NDCs
61919-904-30- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?