NDC 70710-1131 – Chlorpromazine hydrochloride
Chlorpromazine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC70710-1131
Product details
- Brand name
- Chlorpromazine hydrochloride
- Generic name
- Chlorpromazine hydrochloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213368
- Marketed since
- January 27, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phenothiazine
Active ingredients
- Chlorpromazine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1131-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70710-1131-1) | Jan 27, 2020 |
| 70710-1131-4 | 10 BLISTER PACK in 1 CARTON (70710-1131-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1131-2) | Jan 27, 2020 |
Recalls mentioning this NDC
- D-0636-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0634-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0632-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0630-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0638-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0361-2025 Apr 16, 2025 · Class II
CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
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