clopidogrel

Generic: clopidogrel bisulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0080
Product ID 71335-0080_1de06f75-f138-4f1d-b71e-ad82b549d41b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090540
Listing Expiration 2026-12-31
Marketing Start 2012-05-17

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 713350080
Hyphenated Format 71335-0080

Supplemental Identifiers

RxCUI
309362
UNII
08I79HTP27

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 bisulfate (source: ndc)
Application Number ANDA090540 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0080-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0080-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0080-3)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-0080-4)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-0080-5)
source: ndc

Packages (5)

71335-0080-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0080-1) 71335-0080-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-0080-2) 71335-0080-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-0080-3) 71335-0080-4 20 TABLET, FILM COATED in 1 BOTTLE (71335-0080-4) 71335-0080-5 10 TABLET, FILM COATED in 1 BOTTLE (71335-0080-5)

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": "1de06f75-f138-4f1d-b71e-ad82b549d41b", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["e8f98886-4771-4be3-8b57-edfbbc1b4661"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0080-1)", "package_ndc": "71335-0080-1", "marketing_start_date": "20230421"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0080-2)", "package_ndc": "71335-0080-2", "marketing_start_date": "20230502"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0080-3)", "package_ndc": "71335-0080-3", "marketing_start_date": "20240529"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0080-4)", "package_ndc": "71335-0080-4", "marketing_start_date": "20240529"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-0080-5)", "package_ndc": "71335-0080-5", "marketing_start_date": "20240529"}], "brand_name": "Clopidogrel", "product_id": "71335-0080_1de06f75-f138-4f1d-b71e-ad82b549d41b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "71335-0080", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA090540", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}