Chlorpromazine Hydrochloride (Page 5 of 5)

Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature.] Protect from light and moisture.

This package is not for household dispensing. If dispensed for outpatient use, a well closed, light-resistant, child-resistant container should be utilized.

Keep out of reach of children.

Rx only

Manufactured by
UPSHER-SMITH LABORATORIES, LLC
Maple Grove, MN 55369

Revised 1219

DRUG: Chlorpromazine Hydrochloride

GENERIC: Chlorpromazine Hydrochloride

DOSAGE: TABLET, SUGAR COATED

ADMINSTRATION: ORAL

NDC: 70518-0016-0

NDC: 70518-0016-1

NDC: 70518-0016-2

COLOR: brown

SHAPE: ROUND

SCORE: No score

SIZE: 10 mm

IMPRINT: 832;50

PACKAGING: 30 in 1 BLISTER PACK

PACKAGING: 100 in 1 BOX

PACKAGING: 1 in 1 POUCH

ACTIVE INGREDIENT(S):

  • Chlorpromazine Hydrochloride 50mg in 1

INACTIVE INGREDIENT(S):

  • Acacia
  • Shellac
  • Methylparaben
  • Povidone, Unspecified
  • Magnesium Stearate
  • Sucrose
  • Propylparaben
  • Sodium Benzoate
  • Anhydrous Lactose
  • Calcium Sulfate, Unspecified form
  • Carnauba Wax
  • D&C Yellow NO. 10
  • Ferrosoferric oxide
  • Aluminum Oxide
  • FD&C Blue NO. 2
  • FD&C Yellow NO. 6
  • Titanium Dioxide
Remedy_Label
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MM2
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MM3
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CHLORPROMAZINE HYDROCHLORIDE
chlorpromazine hydrochloride tablet, sugar coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70518-0016(NDC:0832-0302)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE) CHLORPROMAZINE HYDROCHLORIDE 50 mg
Inactive Ingredients
Ingredient Name Strength
ACACIA
FERROSOFERRIC OXIDE
CALCIUM SULFATE, UNSPECIFIED FORM
CARNAUBA WAX
D&C YELLOW NO. 10
ALUMINUM OXIDE
FD&C BLUE NO. 2
FD&C YELLOW NO. 6
ANHYDROUS LACTOSE
MAGNESIUM STEARATE
METHYLPARABEN
SHELLAC
POVIDONE, UNSPECIFIED
PROPYLPARABEN
SODIUM BENZOATE
SUCROSE
TITANIUM DIOXIDE
Product Characteristics
Color brown (Butterscotch) Score no score
Shape ROUND Size 10mm
Flavor Imprint Code 832;50
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70518-0016-0 30 TABLET, SUGAR COATED in 1 BLISTER PACK None
2 NDC:70518-0016-1 100 POUCH in 1 BOX contains a POUCH (70518-0016-2)
2 NDC:70518-0016-2 1 TABLET, SUGAR COATED in 1 POUCH This package is contained within the BOX (70518-0016-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA084113 11/25/2016
Labeler — REMEDYREPACK INC. (829572556)

Revised: 02/2020 REMEDYREPACK INC.

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