clopidogrel

Generic: clopidogrel

Labeler: vensun pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel
Labeler vensun pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Vensun Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 42543-713
Product ID 42543-713_4b480542-0dd3-4694-9d43-d5fdcdd64a0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204165
Listing Expiration 2026-12-31
Marketing Start 2014-11-01

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 42543713
Hyphenated Format 42543-713

Supplemental Identifiers

RxCUI
309362 749196
UPC
0342543714304 0342543713307
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 ANDA204165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42543-713-01)
  • 500 TABLET in 1 BOTTLE (42543-713-05)
  • 1000 TABLET in 1 BOTTLE (42543-713-10)
  • 30 TABLET in 1 BOTTLE (42543-713-30)
  • 90 TABLET in 1 BOTTLE (42543-713-90)
source: ndc

Packages (5)

42543-713-01 100 TABLET in 1 BOTTLE (42543-713-01) 42543-713-05 500 TABLET in 1 BOTTLE (42543-713-05) 42543-713-10 1000 TABLET in 1 BOTTLE (42543-713-10) 42543-713-30 30 TABLET in 1 BOTTLE (42543-713-30) 42543-713-90 90 TABLET in 1 BOTTLE (42543-713-90)

Ingredients (1)

clopidogrel bisulfate (75 mg/1)

Linked Drug Pages (1)

Clopidogrel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b480542-0dd3-4694-9d43-d5fdcdd64a0f", "openfda": {"upc": ["0342543714304", "0342543713307"], "unii": ["08I79HTP27"], "rxcui": ["309362", "749196"], "spl_set_id": ["86ee71f2-850e-4c8e-87f3-c7a618d59d95"], "manufacturer_name": ["Vensun Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42543-713-01)", "package_ndc": "42543-713-01", "marketing_start_date": "20141101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42543-713-05)", "package_ndc": "42543-713-05", "marketing_start_date": "20141101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42543-713-10)", "package_ndc": "42543-713-10", "marketing_start_date": "20141101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (42543-713-30)", "package_ndc": "42543-713-30", "marketing_start_date": "20141101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42543-713-90)", "package_ndc": "42543-713-90", "marketing_start_date": "20141101"}], "brand_name": "Clopidogrel", "product_id": "42543-713_4b480542-0dd3-4694-9d43-d5fdcdd64a0f", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "42543-713", "generic_name": "clopidogrel", "labeler_name": "Vensun Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA204165", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}