Klonopin: Package Insert and Label Information (Page 5 of 5)

PRINCIPAL DISPLAY PANEL — 0.5 mg Tablet Bottle Label

NDC 61269-605-10

Klonopin^®
(clonazepam)
CIV

0.5 mg

Each tablet contains 0.5 mg clonazepam.

ATTENTION PHARMACIST: Dispense the
accompanying Medication Guide to each patient.

For additional Medication Guides visitwww.h2-pharma.com/products/klonopin/medicationguide.

100 tablets

Rx only

CHEPLAPHARM Arzneimittel

PRINCIPAL DISPLAY PANEL — 1 mg Tablet Bottle Label

NDC 61269-610-10

Klonopin^®
(clonazepam)
CIV

1 mg

Each tablet contains 1 mg clonazepam.

ATTENTION PHARMACIST: Dispense the
accompanying Medication Guide to each patient.

For additional Medication Guides visitwww.h2-pharma.com/products/klonopin/medicationguide.

100 tablets

Rx only

CHEPLAPHARM Arzneimittel

PRINCIPAL DISPLAY PANEL — 2 mg Tablet Bottle Label

NDC 61269-620-10

Klonopin^®
(clonazepam)
CIV

2 mg

Each tablet contains 2 mg clonazepam.

ATTENTION PHARMACIST: Dispense the
accompanying Medication Guide to each patient.

For additional Medication Guides visitwww.h2-pharma.com/products/klonopin/medicationguide.

100 tablets

Rx only

CHEPLAPHARM Arzneimittel

KLONOPIN clonazepam tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61269-605 Route of Administration ORAL DEA Schedule CIV

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLONAZEPAM (CLONAZEPAM) CLONAZEPAM 0.5 mg

Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE STARCH, CORN FD&C YELLOW NO. 6

Product Characteristics Color ORANGE Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code 1;2;KLONOPIN Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:61269-605-10 100 TABLET in 1 BOTTLE, PLASTIC None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA017533 06/02/1975

KLONOPIN clonazepam tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61269-610 Route of Administration ORAL DEA Schedule CIV

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLONAZEPAM (CLONAZEPAM) CLONAZEPAM 1 mg

Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE STARCH, CORN FD&C BLUE NO. 1 FD&C BLUE NO. 2

Product Characteristics Color BLUE Score no score Shape ROUND Size 9mm Flavor Imprint Code 1;KLONOPIN Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:61269-610-10 100 TABLET in 1 BOTTLE, PLASTIC None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA017533 06/02/1975

KLONOPIN clonazepam tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61269-620 Route of Administration ORAL DEA Schedule CIV

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

Inactive Ingredients Ingredient Name Strength LACTOSE, UNSPECIFIED FORM MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE STARCH, CORN

Product Characteristics Color WHITE Score no score Shape ROUND Size 9mm Flavor Imprint Code 2;KLONOPIN Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:61269-620-10 100 TABLET in 1 BOTTLE, PLASTIC None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA017533 06/02/1975

Labeler — H2-Pharma, LLC (028473634)

Registrant — CHEPLAPHARM Arzneimittel GmbH (329834878)

Revised: 01/2023 H2-Pharma, LLC