NDC 70518-3674
Chlorpromazine Hydrochloride 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-6019.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Makes it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
Product details
- Generic drug
- Chlorpromazine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA084113
- On the market since
- Mar 6, 2023
- Package NDCs
70518-3674-070518-3674-170518-3674-270518-3674-370518-3674-4- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2026
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