clopidogrel

Generic: clopidogrel bisulfate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-073
Product ID 71205-073_3d0c235a-ed00-4295-91a1-c0af34ff07a5
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 71205073
Hyphenated Format 71205-073

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
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-073-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-073-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-073-90)
source: ndc

Packages (3)

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": "3d0c235a-ed00-4295-91a1-c0af34ff07a5", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["ec296eed-81d0-4c1e-bff4-431851899157"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-073-30)", "package_ndc": "71205-073-30", "marketing_start_date": "20180702"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-073-60)", "package_ndc": "71205-073-60", "marketing_start_date": "20180702"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-073-90)", "package_ndc": "71205-073-90", "marketing_start_date": "20180702"}], "brand_name": "Clopidogrel", "product_id": "71205-073_3d0c235a-ed00-4295-91a1-c0af34ff07a5", "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": "71205-073", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Proficient Rx LP", "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"}