Fluphenazine Hydrochloride

Product NDC
71205-839
11-digit product format
712050839
Labeler code
71205
Product ID
71205-839_bc22941e-d2e7-4165-91ea-7239c8b9882d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluphenazine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA215848
Marketing category
ANDA
Marketing start
2022-08-01
Substance
FLUPHENAZINE HYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Phenothiazine [EPC], Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
ZOU145W1XLFLUPHENAZINE HYDROCHLORIDE146-56-5FLUPHENAZINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71205-839-0071205083900100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-00) 2023-02-21NoNoHistorical
71205-839-11712050839111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-11) 2023-02-21NoNoHistorical
71205-839-307120508393030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-30) 2023-02-21NoNoHistorical
71205-839-5571205083955500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-55) 2023-02-21NoNoHistorical
71205-839-607120508396060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-60) 2023-02-21NoNoHistorical
71205-839-6471205083964240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-64) 2023-02-21NoNoHistorical
71205-839-7271205083972120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-72) 2023-02-21NoNoHistorical
71205-839-7871205083978180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-78) 2023-02-21NoNoHistorical
71205-839-907120508399090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-839-90) 2023-02-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Fluphenazine Hydrochloride Tablets, USPProficient Rx LP2023-02-01HUMAN PRESCRIPTION DRUG LABEL1