NDC 54868-4055
Venlafaxine Hydrochloride 37.5 mg tablet
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-393.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ALKALOIDA Vegyeszeti Gyar zartkoruen mukodo Reszvenytarsasag | Tiszavasvari, Hungary | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 12, 2025 · 6 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet
- Strength
- 37.5 mg
- Approval
- ANDA ANDA078627
- On the market since
- Jul 19, 2007
- Package NDCs
54868-4055-054868-4055-154868-4055-254868-4055-3- Official label
- DailyMed (National Library of Medicine), updated Mar 4, 2012
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