NDC 71205-838 – Fluphenazine Hydrochloride

Fluphenazine Hydrochloride 2.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-838

Product details

Brand name
Fluphenazine Hydrochloride
Generic name
Fluphenazine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215848
Marketed since
August 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Fluphenazine Hydrochloride →

Package NDC codes (9)

Package NDCDescriptionSince
71205-838-00100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-00)Feb 21, 2023
71205-838-111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-11)Feb 21, 2023
71205-838-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-30)Feb 21, 2023
71205-838-55500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-55)Feb 21, 2023
71205-838-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-60)Feb 21, 2023
71205-838-64240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-64)Feb 21, 2023
71205-838-72120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-72)Feb 21, 2023
71205-838-78180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-78)Feb 21, 2023
71205-838-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-838-90)Feb 21, 2023

Other Fluphenazine Hydrochloride products