clopidogrel

Generic: clopidogrel

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

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4138
Product ID 68071-4138_2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076999
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 680714138
Hyphenated Format 68071-4138

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 (source: ndc)
Application Number ANDA076999 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)
source: ndc

Packages (1)

68071-4138-3 30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)

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": "2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["5cdca9bd-7042-142a-e053-2991aa0a9ca6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)", "package_ndc": "68071-4138-3", "marketing_start_date": "20171031"}], "brand_name": "Clopidogrel", "product_id": "68071-4138_2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5", "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": "68071-4138", "generic_name": "Clopidogrel", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA076999", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}