Chlorpromazine Hydrochloride 16714-0048
Product NDC
16714-0048- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 11, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA213368
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 25 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE (16714-048-01)