Manufactured for:
Abbott Laboratories
North Chicago, IL. 60064
USA

LB0024-08     Rev. 11/10

PRINCIPAL DISPLAY PANEL - 120 mg Bottle Label
NDC 0074-3045-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets

120 mg

30 Tablets

Rx
ONLY

Abbott

PRINCIPAL DISPLAY PANEL - 180 mg Bottle Label
NDC 0074-3061-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets
180 mg
30 Tablets

Rx
ONLY

Abbott

PRINCIPAL DISPLAY PANEL - 240 mg Bottle Label
NDC 0074-3062-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets

240 mg

30 Tablets

Rx
ONLY

Abbott

PRINCIPAL DISPLAY PANEL - 300 mg Bottle Label
NDC 0074-3063-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets

300 mg

30 Tablets

Rx
ONLY

Abbott

PRINCIPAL DISPLAY PANEL - 360 mg Bottle Label
NDC 0074-3064-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets

360 mg

30 Tablets

Rx
ONLY

Abbott

PRINCIPAL DISPLAY PANEL - 420 mg Bottle Label
NDC 0074-3069-30

CARDIZEM® LA
(Diltiazem Hydrochloride)
Extended Release Tablets

420 mg

30 Tablets

Rx
ONLY

Abbott

CARDIZEM LA 
diltiazem hydrochloride   tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0074-3045
Route of Administration ORAL DEA Schedule      
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Diltiazem Hydrochloride (Diltiazem)  Diltiazem Hydrochloride 120 mg
Inactive Ingredients
Ingredient Name Strength
carnauba wax  
silicon dioxide  
croscarmellose sodium  
ethyl acrylate - methyl methacrylate copolymer  
hypromelloses  
magnesium stearate  
cellulose, microcrystalline  
microcrystalline wax  
polydextrose  
polyethylene glycol  
polysorbate 80  
povidone  
sucrose stearate  
talc  
titanium dioxide  
Product Characteristics
Color WHITE Score no score 
Shape OVAL (Capsule-shaped)  Size 13mm
Flavor  Imprint Code B;120;mg 
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0074-3045-30 30 TABLET In 1 BOTTLE None
2 0074-3045-90 90 TABLET In 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021392 12/25/2010 
CARDIZEM LA 
diltiazem hydrochloride   tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0074-3061
Route of Administration ORAL DEA Schedule      
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Diltiazem Hydrochloride (Diltiazem)  Diltiaz