NDC 60687-419
Chlorpromazine Hydrochloride 10 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Amneal Pharmaceuticals's NDC 69238-1054.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Amneal Pharmaceuticals names for other drugs.
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Aug 18, 2025 · Class II · Amneal Pharmaceuticals, LLC
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Lots: Lot AM240617, AM240618, Exp Date 04/30/2027 - Aug 18, 2025 · Class II · Amneal Pharmaceuticals, LLC
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Lots: Lot: AM240147, AM240148, Exp Date 01/31/2027; Lot AM240664, AM240665, Exp Date 04/30/2027. - Aug 18, 2025 · Class II · Amneal Pharmaceuticals, LLC
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Lots: Lot: AM240334, AM240335, Exp Date 02/28/2027, AM241031, Exp Date 06/30/2027. - Aug 18, 2025 · Class II · Amneal Pharmaceuticals, LLC
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Lots: Lot: AM240336, AM240337, Exp Date 02/28/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Chlorpromazine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA209755
- On the market since
- Jun 13, 2019
- Package NDCs
60687-419-0160687-419-11- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2026
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