NDC 69238-1058 – Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC69238-1058
Product details
- Brand name
- Chlorpromazine Hydrochloride
- Generic name
- Chlorpromazine Hydrochloride
- Labeler
- Amneal Pharmaceuticals NY LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209755
- Marketed since
- September 12, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phenothiazine
Active ingredients
- Chlorpromazine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69238-1058-1 | 100 TABLET, FILM COATED in 1 BOTTLE (69238-1058-1) | Sep 12, 2018 |
Recalls mentioning this NDC
- D-0616-2025 Sep 10, 2025 · Class II
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. - D-0617-2025 Sep 10, 2025 · Class II
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. - D-0619-2025 Sep 10, 2025 · Class II
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. - D-0618-2025 Sep 10, 2025 · Class II
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.
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