Chlorpromazine Hydrochloride 68462-0863
Product NDC
68462-0863- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 23, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA212144
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 50 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (68462-863-01)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-863-10)