Venlafaxine (Page 12 of 12)

Package/Label Display Panel – Carton – 25 mg

NDC 68084- 896 -25

Venlafaxine
Tablets, USP

25 mg

30 Tablets (5 × 6)                Rx Only

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

Each Tablet Contains:
Venlafaxine hydrochloride, USP equivalent to
venlafaxine………………………………………………25 mg

Usual Dosage: See package insert for full
prescribing information.

Store at 20º to 25ºC (68º to 77ºF) in a dry place;
excursions permitted between 15º to 30ºC (59º to
86ºF) [see USP Controlled Room Temperature].

Keep this and all drugs out of reach of
children.

FOR YOUR PROTECTION: Do not use if blister is
torn or broken.

The drug product contained in this package is
from NDC # 68001-157, BluePoint Laboratories.

Distributed by:
American Health Packaging
Columbus, Ohio 43217

089625 0289625/0319OS

Package/Label Display Panel – Blister – 25 mg

Venlafaxine Tablet, USP

25 mg

Package/Label Display Panel – Carton – 37.5 mg

NDC 68084- 844 -01

Venlafaxine
Tablets, USP

37.5 mg

100 Tablets (10 × 10)                Rx Only

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

Each Tablet Contains:
Venlafaxine hydrochloride, USP equivalent to venlafaxine…….37.5 mg

Usual Dosage: See package insert for complete prescribing information.

Store at 20º to 25ºC (68º to 77ºF) in a dry place; excursions permitted
between 15º to 30ºC (59º to 86ºF) [see USP Controlled Room
Temperature].

Keep this and all drugs out of reach of children.

FOR YOUR PROTECTION: Do not use if blister is torn or broken.

The drug product contained in this package is from
NDC # 68001-158, BluePoint Laboratories.

Distributed by:
American Health Packaging
Columbus, Ohio 43217

084401 0284401/0320

Package/Label Display Panel – Blister – 37.5 mg

Venlafaxine Tablet, USP

37.5 mg

Package/Label Display Panel – Carton – 75 mg

NDC 68084- 856 -01

Venlafaxine
Tablets, USP

75 mg

100 Tablets (10 × 10)                Rx Only

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

Each Tablet Contains:
Venlafaxine hydrochloride, USP equivalent to venlafaxine 75 mg

Usual Dosage: See package insert for full prescribing
information.

Store at 20º to 25ºC (68º to 77ºF) in a dry place; excursions
permitted between 15° to 30°C (59° to 86°F) [See USP Controlled
Room Temperature].

Keep this and all drugs out of reach of children.

FOR YOUR PROTECTION: Do not use if blister is torn or broken.

The drug product contained in this package is from
NDC # 68001-160, BluePoint Laboratories.

Packaged and Distributed by:
American Health Packaging
Columbus, Ohio 43217

085601 0285601/0419

Package/Label Display Panel – Blister – 75 mg

Venlafaxine Tablet, USP

75 mg

VENLAFAXINE venlafaxine tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68084-896(NDC:68001-157) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 25 mg

Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED FERRIC OXIDE YELLOW LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics Color orange (PEACH) Score 2 pieces Shape ROUND (ROUND) Size 6mm Flavor Imprint Code ZC;64 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:68084-896-25 30 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (68084-896-95) 1 NDC:68084-896-95 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (68084-896-25)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077653 02/15/2015

VENLAFAXINE venlafaxine tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68084-844(NDC:68001-158) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 37.5 mg

Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED FERRIC OXIDE YELLOW LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics Color orange (PEACH) Score 2 pieces Shape ROUND (ROUND) Size 7mm Flavor Imprint Code ZC;65 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:68084-844-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (68084-844-11) 1 NDC:68084-844-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (68084-844-01)

(click image for full-size original)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077653 04/17/2015

VENLAFAXINE venlafaxine tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68084-856(NDC:68001-160) Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE) VENLAFAXINE 75 mg

Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED FERRIC OXIDE YELLOW LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A POTATO

Product Characteristics Color orange (PEACH) Score 2 pieces Shape ROUND (ROUND) Size 10mm Flavor Imprint Code ZC;67 Contains

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:68084-856-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE contains a BLISTER PACK (68084-856-11) 1 NDC:68084-856-11 1 TABLET in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (68084-856-01)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077653 03/06/2015

Labeler — American Health Packaging (929561009)

Establishment
Name	Address	ID/FEI	Operations
American Health Packaging		929561009	repack (68084-844), repack (68084-896), repack (68084-856)

Revised: 09/2020 American Health Packaging