Aripiprazole (Page 11 of 11)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50268-087-12
Aripiprazole Tablets
2 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026808712
NDC 50268-087-12
Aripiprazole Tablets
2 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026808712

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 2 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE
Mfg. Rev. 2028680 AV 04/16 (P)

NDC 50268-088-15
Aripiprazole Tablets
5 mg
Rx Only
50 Tablets (5 x 10) Unit Dose
5026808815
NDC 50268-088-15
Aripiprazole Tablets
5 mg
Rx Only
50 Tablets (5 x 10) Unit Dose
5026808815

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 5 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE Mfg. Rev. 2028681 AV 04/16 (P)

NDC 50268-089-15
Aripiprazole Tablets
10 mg
Rx Only
50 Tablets (5 x 10) Unit Dose
5026808915
NDC 50268-089-15
Aripiprazole Tablets
10 mg
Rx Only
50 Tablets (5 x 10) Unit Dose
5026808915

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 10 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE Mfg. Rev. 2028682 AV 04/16 (P)

NDC 50268-090-12
Aripiprazole Tablets
15 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809012
NDC 50268-090-12
Aripiprazole Tablets
15 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809012

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 15 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE Mfg. Rev. 2028683 AV 04/16 (P)

NDC 50268-091-12
Aripiprazole Tablets
20 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809112
NDC 50268-091-12
Aripiprazole Tablets
20 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809112

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 20 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE Mfg. Rev. 2028684 AV 04/16 (P)

NDC 50268-092-12
Aripiprazole Tablets
30 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809212
NDC 50268-092-12
Aripiprazole Tablets
30 mg
Rx Only
20 Tablets (2 x 10) Unit Dose
5026809212

Pharmacist: Dispense the Medication Guide provided separately to each patient.
Each tablet contains 30 mg of aripiprazole.
Usual Dosage: See package insert for full prescribing information.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
Contact Number: 1-855-361-3993
KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Manufactured for:
AvKARE, Inc.
Pulaski, TN 38478

AvPAK
A PRODUCT of AvKARE Mfg. Rev. 2028685 AV 04/16 (P)

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-087(NDC:31722-819) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 2 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color green Score no score Shape RECTANGLE Size 8mm Flavor Imprint Code I;94 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-087-12 20 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-087-11) 1 NDC:50268-087-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-087-12)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-088(NDC:31722-820) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 5 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color blue Score no score Shape RECTANGLE Size 8mm Flavor Imprint Code I;95 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-088-15 50 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-088-11) 1 NDC:50268-088-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-088-15)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-089(NDC:31722-827) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 10 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color pink Score no score Shape RECTANGLE Size 8mm Flavor Imprint Code I;96 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-089-15 50 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-089-11) 1 NDC:50268-089-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-089-15)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-090(NDC:31722-828) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 15 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color yellow Score no score Shape ROUND Size 7mm Flavor Imprint Code I;97 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-090-12 20 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-090-11) 1 NDC:50268-090-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-090-12)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-091(NDC:31722-829) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 20 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color white (off-white) Score no score Shape ROUND Size 7mm Flavor Imprint Code I;98 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-091-12 20 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-091-11) 1 NDC:50268-091-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-091-12)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

ARIPIPRAZOLE aripiprazole tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50268-092(NDC:31722-830) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARIPIPRAZOLE (ARIPIPRAZOLE) ARIPIPRAZOLE 30 mg

Inactive Ingredients Ingredient Name Strength STARCH, CORN FD&C BLUE NO. 2 FERRIC OXIDE RED FERRIC OXIDE YELLOW HYPROMELLOSES LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE

Product Characteristics Color pink Score no score Shape ROUND Size 9mm Flavor Imprint Code I;99 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50268-092-12 20 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (50268-092-11) 1 NDC:50268-092-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (50268-092-12)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA205064 04/28/2016

Labeler — AvPAK (832926666)

Revised: 01/2022 AvPAK