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NDC 50090-2082-01 Clopidogrel 75 mg/1 Details
Clopidogrel 75 mg/1
Clopidogrel is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is CLOPIDOGREL BISULFATE.
MedlinePlus Drug Summary
Clopidogrel is used alone or with aspirin to prevent serious or life-threatening problems with the heart and blood vessels in people who have had a stroke, heart attack, or severe chest pain. This includes people who have percutaneous coronary intervention (PCI; angioplasty; a type of heart surgery) that may involve inserting coronary stents (metal tubes surgically placed in clogged blood vessels to improve blood flow) or who have coronary artery bypass grafting (CABG; a type of heart surgery). Clopidogrel is also used to prevent serious or life-threatening problems with the heart and blood vessels in people who have peripheral arterial disease (poor circulation in the blood vessels that supply blood to the legs). Clopidogrel is in a class of medications called antiplatelet medications. It works by preventing platelets (a type of blood cell) from collecting and forming clots that may cause a heart attack or stroke.
Related Packages: 50090-2082-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clopidogrel
Product Information
NDC | 50090-2082 |
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Product ID | 50090-2082_6bfb4a82-234b-430f-a3bd-f235bcbedb2f |
Associated GPIs | 85158020100320 |
GCN Sequence Number | 038164 |
GCN Sequence Number Description | clopidogrel bisulfate TABLET 75 MG ORAL |
HIC3 | M9P |
HIC3 Description | PLATELET AGGREGATION INHIBITORS |
GCN | 96010 |
HICL Sequence Number | 017539 |
HICL Sequence Number Description | CLOPIDOGREL BISULFATE |
Brand/Generic | Generic |
Proprietary Name | Clopidogrel |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Clopidogrel Bisulfate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 75 |
Active Ingredient Units | mg/1 |
Substance Name | CLOPIDOGREL BISULFATE |
Labeler Name | A-S Medication Solutions |
Pharmaceutical Class | Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA090540 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50090-2082-01 (50090208201)
NDC Package Code | 50090-2082-1 |
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Billing NDC | 50090208201 |
Package | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2082-1) |
Marketing Start Date | 2015-10-08 |
NDC Exclude Flag | N |
Pricing Information | N/A |