Fluphenazine Hydrochloride

Product NDC
71205-840
11-digit product format
712050840
Labeler code
71205
Product ID
71205-840_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
10 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
71205-840-0071205084000100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-00) 2023-02-21NoNoHistorical
71205-840-11712050840111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-11) 2023-02-21NoNoHistorical
71205-840-307120508403030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-30) 2023-02-21NoNoHistorical
71205-840-5571205084055500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-55) 2023-02-21NoNoHistorical
71205-840-607120508406060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-60) 2023-02-21NoNoHistorical
71205-840-6471205084064240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-64) 2023-02-21NoNoHistorical
71205-840-7271205084072120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-72) 2023-02-21NoNoHistorical
71205-840-7871205084078180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-78) 2023-02-21NoNoHistorical
71205-840-907120508409090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-840-90) 2023-02-21NoNoHistorical

Related DailyMed Labels

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