NDC 70518-4065
Venlafaxine Hydrochloride 75 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-579.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it | Problems found, fixed voluntarilyOct 23, 2022 · 6 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA216044
- On the market since
- May 4, 2024
- Package NDCs
70518-4065-0- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
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