Chlorpromazine Hydrochloride 70518-4295
Product NDC
70518-4295- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 26, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA084115
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 200 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
100 POUCH in 1 BOX (70518-4295-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4295-1)