NDC 16714-047 – Chlorpromazine hydrochloride
Chlorpromazine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC16714-047
Product details
- Brand name
- Chlorpromazine hydrochloride
- Generic name
- Chlorpromazine hydrochloride
- Labeler
- Northstar Rx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA213368
- Marketed since
- May 11, 2020
- Marketing end
- November 30, 2026
- Pharmacologic class
- Phenothiazine
Active ingredients
- Chlorpromazine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-047-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-047-01) | May 11, 2020 |
Recalls mentioning this NDC
- D-0633-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0631-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0635-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0637-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit - D-0639-2025 Sep 17, 2025 · Class II
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
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