Clopidogrel Kit (Page 6 of 6)

Clopidogrel Tablets, USP 75 mg

Clopidogrel Tablets, USP 75mg
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CLOPIDOGREL KIT clopidogrel kit kit
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70882-123
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-123-01 1 KIT in 1 KIT None
Quantity of Parts
Part # Package Quantity Total Product Quantity
Part 1 1 BLISTER PACK 30
Part 2 1 BLISTER PACK 30
Part 1 of 2
CLOPIDOGREL clopidogrel bisulfate tablet, film coated
Product Information
Item Code (Source) NDC:70882-116
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLOPIDOGREL BISULFATE (CLOPIDOGREL) CLOPIDOGREL 75 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
SILICON DIOXIDE
CROSPOVIDONE, UNSPECIFIED
METHYLCELLULOSE (15 MPA.S)
ZINC STEARATE
FERRIC OXIDE RED
HYDROXYPROPYL CELLULOSE (1200000 MW)
HYPROMELLOSE, UNSPECIFIED
POLYETHYLENE GLYCOL 8000
TITANIUM DIOXIDE
Product Characteristics
Color PINK Score no score
Shape ROUND Size 9mm
Flavor Imprint Code APO;CL;75
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-116-30 30 TABLET, FILM COATED in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076274 07/01/2017
Part 2 of 2
ASPIRINLOW DOSE LOW DOSE aspirin tablet, coated
Product Information
Item Code (Source) NDC:70882-122
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPIRIN (ASPIRIN) ASPIRIN 81 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
HYPROMELLOSE, UNSPECIFIED
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE
SODIUM BICARBONATE
SODIUM LAURYL SULFATE
TALC
TITANIUM DIOXIDE
TRIACETIN
METHACRYLIC ACID
POLYDEXTROSE
TRIETHYL CITRATE
POLYETHYLENE GLYCOL, UNSPECIFIED
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 6mm
Flavor Imprint Code L
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70882-122-30 30 TABLET, COATED in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part343 07/01/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076274 07/01/2017
Labeler — Cambridge Therapeutics Technologies, LLC (080072003)

Revised: 07/2017 Cambridge Therapeutics Technologies, LLC

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