Enalapril Maleate (Page 6 of 6)

HOW SUPPLIED

Enalapril Maleate Tablets

NDC

Strength

Quantity

Description

68788-7309-3

68788-7309-6

68788-7309-9

68788-7309-1

20 mg

Bottles of 30

Bottles of 60

Bottles of 90

Bottles of 100

Peach, rounded triangle shaped tablet imprinted with “VASO 20” on one side and scored on the other.

Storage

Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Keep container tightly closed. Protect from moisture.Dispense in a tight container as per USP, if product package is subdivided.

Distributed by:

Oceanside Pharmaceuticals, a division of

Bausch Health US, LLC

Bridgewater, NJ 08807 USA

Manufactured by:

Bausch Health Companies Inc.

Steinbach, MB R5G 1Z7, Canada

© 2020 Bausch Health Companies Inc. or its affiliates

9450104_20003098

Rev. 12/2020

Repackaged By: Preferred Pharmaceuticals Inc.

PRINCIPAL DISPLAY PANEL – 20 mg

Enalapril Maleate Tablets USP 20mg
(click image for full-size original)

NDC 68788-7909

Rx only

Enalapril Maleate Tablets

20 mg

OCEANSIDE PHARMACEUTICALS

Repackaged By: Preferred Pharmaceuticals Inc.

ENALAPRIL MALEATE enalapril maleate tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68788-7309(NDC:68682-713)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Enalapril Maleate (Enalaprilat Anhydrous) Enalapril Maleate 20 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE, UNSPECIFIED FORM
magnesium stearate
sodium stearate
sodium bicarbonate
starch, corn
ferric oxide red
ferric oxide yellow
Product Characteristics
Color PINK (Pink Peach color) Score 2 pieces
Shape TRIANGLE (rounded triangle) Size 8mm
Flavor Imprint Code VASO;20
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68788-7309-3 30 TABLET in 1 BOTTLE None
2 NDC:68788-7309-6 60 TABLET in 1 BOTTLE None
3 NDC:68788-7309-9 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA authorized generic NDA018998 01/04/2019
Labeler — Preferred Pharmaceuticals Inc. (791119022)
Registrant — Preferred Pharmaceuticals Inc. (791119022)
Establishment
Name Address ID/FEI Operations
Preferred Pharmaceuticals Inc. 791119022 REPACK (68788-7309)

Revised: 05/2022 Preferred Pharmaceuticals Inc.

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