NDC 0832-6019
Chlorpromazine Hydrochloride 50 mg tablet, film coated
On the label: Upsher-Smith Laboratories, Inc..
Where it's 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
- Aug 3, 2011
- Package NDCs
0832-6019-000832-6019-010832-6019-100832-6019-89- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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