Minds On Meds

Mental Health Medications

Antipsychotics

Thioridazine Hydrochloride, Page 3

Thioridazine is indicated for the management of schizophrenic patients who fail to respond adequately to treatment with other antipsychotic drugs. Due to the risk of significant, potentially life threatening, proarrhythmic effects with thioridazine treatment, thioridazine should be used only in patients who have failed to respond adequately to treatment with appropriate courses of other antipsychotic drugs.

PRINCIPAL DISPLAY PANEL -10 mg Bottle Label

MP

NDC53489-148-01

THIORIDAZINE HCl
TABLETS USP

10 mg

100 TABLETS

Rx only

MUTUAL PHARMACEUTICAL CO., INC.
PHILADELPHIA, PA 19124 USA

PRINCIPAL DISPLAY PANEL -10 mg Bottle Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 25 mg Bottle Label

MP

NDC53489-149-01

THIORIDAZINE HCl
TABLETS USP

25 mg

100 TABLETS

Rx only

MUTUAL PHARMACEUTICAL CO., INC.
PHILADELPHIA, PA 19124 USA

PRINCIPAL DISPLAY PANEL -- 25 mg Bottle Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 50 mg Bottle Label

MP

NDC53489-150-01

THIORIDAZINE HCl
TABLETS USP

50 mg

100 TABLETS

Rx only

MUTUAL PHARMACEUTICAL CO., INC.
PHILADELPHIA, PA 19124 USA

PRINCIPAL DISPLAY PANEL -- 50 mg Bottle Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 100 mg Bottle Label

MP

NDC53489-500-01

THIORIDAZINE HCl
TABLETS USP

100 mg

100 TABLETS

Rx only

MUTUAL PHARMACEUTICAL CO., INC.
PHILADELPHIA, PA 19124 USA

PRINCIPAL DISPLAY PANEL -- 100 mg Bottle Label
(click image for full-size original)
THIORIDAZINE HYDROCHLORIDE
thioridazine hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-148
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Thioridazine Hydrochloride (Thioridazine) Thioridazine 10 mg
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 6mm
Flavor Imprint Code MP;12
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-148-01 100 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-148-10 1000 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA089953 10/07/1988
THIORIDAZINE HYDROCHLORIDE
thioridazine hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-149
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Thioridazine Hydrochloride (Thioridazine) Thioridazine 25 mg
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 7mm
Flavor Imprint Code MP;14
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-149-01 100 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-149-10 1000 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA089953 10/07/1988
THIORIDAZINE HYDROCHLORIDE
thioridazine hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-150
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Thioridazine Hydrochloride (Thioridazine) Thioridazine 50 mg
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 9mm
Flavor Imprint Code MP;17
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-150-01 100 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-150-10 1000 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA089953 10/07/1988
THIORIDAZINE HYDROCHLORIDE
thioridazine hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53489-500
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Thioridazine Hydrochloride (Thioridazine) Thioridazine 100 mg
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 10mm
Flavor Imprint Code MP;160
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53489-500-60 20 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
2 NDC:53489-500-02 50 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
3 NDC:53489-500-06 60 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
4 NDC:53489-500-01 100 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
5 NDC:53489-500-03 250 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
6 NDC:53489-500-05 500 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
7 NDC:53489-500-10 1000 TABLET, FILM COATED (TABLET) in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA089953 10/07/1988
Labeler — Mutual Pharmaceutical (121735955)

Revised: 09/2010 Mutual Pharmaceutical