Chlorpromazine Hydrochloride 71656-0102
Product NDC
71656-0102- Manufacturer
- Saptalis Pharmaceuticals, Llc.
- Dosage Form
- Concentrate
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 4, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA080983
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Chlorpromazine Hydrochloride | 30 mg/mL |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
120 mL in 1 BOTTLE, PLASTIC (71656-102-04)