NDC 31722-901

clopidogrel

Clopidogrel

clopidogrel is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is Clopidogrel Bisulfate.

Product ID31722-901_5ac8bdbe-355f-4271-a45b-cf38522e787d
NDC31722-901
Product TypeHuman Prescription Drug
Proprietary Nameclopidogrel
Generic NameClopidogrel
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-03-03
Marketing CategoryANDA / ANDA
Application NumberANDA204165
Labeler NameCamber Pharmaceuticals, Inc.
Substance NameCLOPIDOGREL BISULFATE
Active Ingredient Strength75 mg/1
Pharm ClassesDecreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 31722-901-90

90 TABLET, FILM COATED in 1 BOTTLE (31722-901-90)
Marketing Start Date2016-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 31722-901-90 [31722090190]

clopidogrel TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204165
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-03-03
Inactivation Date2020-01-31

NDC 31722-901-05 [31722090105]

clopidogrel TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204165
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-03-03
Inactivation Date2020-01-31

NDC 31722-901-01 [31722090101]

clopidogrel TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204165
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-03-03
Inactivation Date2020-01-31

NDC 31722-901-30 [31722090130]

clopidogrel TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204165
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-03-03
Inactivation Date2020-01-31

NDC 31722-901-10 [31722090110]

clopidogrel TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA204165
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-03-03
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CLOPIDOGREL BISULFATE75 mg/1

OpenFDA Data

SPL SET ID:be5aae47-c2d3-4576-8588-a4b09fce91b8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 749196
  • 309362
  • UPC Code
  • 0331722901307
  • Pharmacological Class

    • Decreased Platelet Aggregation [PE]
    • P2Y12 Platelet Inhibitor [EPC]
    • P2Y12 Receptor Antagonists [MoA]
    • Cytochrome P450 2C8 Inhibitors [MoA]

    Medicade Reported Pricing

    31722090190 CLOPIDOGREL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

    31722090130 CLOPIDOGREL 75 MG TABLET

    Pricing Unit: EA | Drug Type:

    31722090105 CLOPIDOGREL 75 MG TABLET

    Pricing Unit: EA | Drug Type: