NDC 50268-166 – Chlorpromazine Hydrochloride
Chlorpromazine Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral
Product NDC50268-166
Product details
- Brand name
- Chlorpromazine Hydrochloride
- Generic name
- Chlorpromazine Hydrochloride
- Labeler
- AvPAK
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209755
- Marketed since
- February 14, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phenothiazine
Active ingredients
- Chlorpromazine Hydrochloride 200 mg/1
Uses, dosage, side effects and warnings for Chlorpromazine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50268-166-12 | 20 BLISTER PACK in 1 BOX (50268-166-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-166-11) | Feb 14, 2020 |
Recalls mentioning this NDC
- D-0644-2025 Sep 17, 2025 · Class II
Presence of a foreign substance. - D-0643-2025 Sep 17, 2025 · Class II
Presence of a foreign substance.
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