Chlorpromazine Hydrochloride 70710-1133
Product NDC
70710-1133- Manufacturer
- Zydus Pharmaceuticals (usa) Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 27, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA213368
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 200 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (70710-1133-1)
10 BLISTER PACK in 1 CARTON (70710-1133-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70710-1133-2)