Fluphenazine Hydrochloride 00121-0654
Product NDC
00121-0654- Manufacturer
- Pai Holdings, Llc Dba Pai Pharma
- Dosage Form
- Elixir
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 31, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA040146
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluphenazine Hydrochloride | .5 mg/mL |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(2)
60 mL in 1 BOTTLE (0121-0654-02)
473 mL in 1 BOTTLE (0121-0654-16)