clopidogrel

Generic: clopidogrel

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel
Labeler amneal pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-414
Product ID 65162-414_360ed8dd-4f92-46fc-b31b-abe0d75e9bb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203751
Listing Expiration 2026-12-31
Marketing Start 2013-09-30

Pharmacologic Class

Classes
cytochrome p450 2c8 inhibitors [moa] decreased platelet aggregation [pe] p2y12 platelet inhibitor [epc] p2y12 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162414
Hyphenated Format 65162-414

Supplemental Identifiers

RxCUI
309362
UNII
08I79HTP27

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name clopidogrel (source: ndc)
Generic Name clopidogrel (source: ndc)
Application Number ANDA203751 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (65162-414-03)
  • 90 TABLET in 1 BOTTLE (65162-414-09)
  • 1000 TABLET in 1 BOTTLE (65162-414-11)
  • 500 TABLET in 1 BOTTLE (65162-414-50)
source: ndc

Packages (4)

Ingredients (1)

clopidogrel bisulfate (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "360ed8dd-4f92-46fc-b31b-abe0d75e9bb3", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["0d010775-1160-4b2e-a928-563a02edd191"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-414-03)", "package_ndc": "65162-414-03", "marketing_start_date": "20130930"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65162-414-09)", "package_ndc": "65162-414-09", "marketing_start_date": "20130930"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65162-414-11)", "package_ndc": "65162-414-11", "marketing_start_date": "20130930"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-414-50)", "package_ndc": "65162-414-50", "marketing_start_date": "20130930"}], "brand_name": "Clopidogrel", "product_id": "65162-414_360ed8dd-4f92-46fc-b31b-abe0d75e9bb3", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "65162-414", "generic_name": "Clopidogrel", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA203751", "marketing_category": "ANDA", "marketing_start_date": "20130930", "listing_expiration_date": "20261231"}