VERAPAMIL HYDROCHLORIDE (Page 5 of 5)

PACKAGE LABEL

Label Image for 53808-1019 180mg

Label Image for 180mgLabel Image for 180mg
VERAPAMIL HYDROCHLORIDE verapamil hydrochloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:53808-1019(NDC:57664-117)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VERAPAMIL HYDROCHLORIDE (VERAPAMIL) VERAPAMIL HYDROCHLORIDE 180 mg
Inactive Ingredients
Ingredient Name Strength
CARNAUBA WAX
HYPROMELLOSES
POLYETHYLENE GLYCOL 8000
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYDEXTROSE
POVIDONES
SODIUM ALGINATE
TITANIUM DIOXIDE
TRIACETIN
D&C YELLOW NO. 10
FERRIC OXIDE YELLOW
Product Characteristics
Color YELLOW Score 2 pieces
Shape OVAL Size 16mm
Flavor Imprint Code 117
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:53808-1019-1 30 TABLET, EXTENDED RELEASE (TABLET) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090529 11/01/2014
Labeler — State of Florida DOH Central Pharmacy (829348114)
Establishment
Name Address ID/FEI Operations
State of Florida DOH Central Pharmacy 829348114 repack (53808-1019)

Revised: 01/2015 State of Florida DOH Central Pharmacy

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