NDC 70518-4295
Chlorpromazine Hydrochloride 200 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 0832-6021.
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
- 200 mg
- Approval
- ANDA ANDA084115
- On the market since
- Feb 26, 2025
- Package NDCs
70518-4295-070518-4295-170518-4295-270518-4295-3- Official label
- DailyMed (National Library of Medicine), updated Sep 3, 2026
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