Fluphenazine Hydrochloride 71205-0839
Product NDC
71205-0839- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 1, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA215848
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluphenazine Hydrochloride | 5 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(9)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-00)
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-11)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-30)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-55)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-60)
240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-64)
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-72)
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-78)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-90)