Valacyclovir Hydrochloride (Page 8 of 8)

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Valacyclovir hydrochloride 1g Tablets #30
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Valacyclovir Hydrochloride Tablets 1 g 90s Label Text

NDC 0093-7259 -98

VALACYCLOVIR

HYDROCHLORIDE

Tablets, 1 g*

PHARMACIST: PLEASE DISPENSE WITH

ATTACHED PATIENT INFORMATION

LEAFLET

Do not use if safety seal under cap is

broken or missing.

Rx only

90 TABLETS

TEVA

VALACYCLOVIR HYDROCHLORIDE
valacyclovir hydrochloride tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66116-516(NDC:0093-7259)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VALACYCLOVIR HYDROCHLORIDE (ACYCLOVIR) VALACYCLOVIR 1 g
Inactive Ingredients
Ingredient Name Strength
POWDERED CELLULOSE
CROSCARMELLOSE SODIUM
FD&C BLUE NO. 2
ALUMINUM OXIDE
HYPROMELLOSE 2910 (6 MPA.S)
STARCH, CORN
POLYETHYLENE GLYCOL 400
POLYSORBATE 80
SODIUM STEARYL FUMARATE
TITANIUM DIOXIDE
Product Characteristics
Color BLUE Score 2 pieces
Shape OVAL (capsule-shaped) Size 23mm
Flavor Imprint Code 93;7259
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66116-516-30 30 TABLET, FILM COATED in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077655 05/24/2010
Labeler — MedVantx, Inc. (806427725)
Registrant — Teva Pharmaceuticals USA Inc (118234421)
Establishment
Name Address ID/FEI Operations
Blenheim Pharmacal, Inc. 171434587 REPACK (66116-516)

Revised: 07/2012 MedVantx, Inc.

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