clopidogrel

Generic: clopidogrel

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

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-7314
Product ID 0093-7314_a9df5ba4-ab12-4f72-9264-a1f7f377e35b
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 00937314
Hyphenated Format 0093-7314

Supplemental Identifiers

RxCUI
309362
UPC
0300937314561
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 ANDA076999 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (0093-7314-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (0093-7314-56)
  • 90 TABLET, FILM COATED in 1 BOTTLE (0093-7314-98)
source: ndc

Packages (3)

0093-7314-05 500 TABLET, FILM COATED in 1 BOTTLE (0093-7314-05) 0093-7314-56 30 TABLET, FILM COATED in 1 BOTTLE (0093-7314-56) 0093-7314-98 90 TABLET, FILM COATED in 1 BOTTLE (0093-7314-98)

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": "a9df5ba4-ab12-4f72-9264-a1f7f377e35b", "openfda": {"upc": ["0300937314561"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["bc747f6d-f52c-4dcb-bda5-2d0a9f954147"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-7314-05)", "package_ndc": "0093-7314-05", "marketing_start_date": "20120517"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7314-56)", "package_ndc": "0093-7314-56", "marketing_start_date": "20120517"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0093-7314-98)", "package_ndc": "0093-7314-98", "marketing_start_date": "20120517"}], "brand_name": "Clopidogrel", "product_id": "0093-7314_a9df5ba4-ab12-4f72-9264-a1f7f377e35b", "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": "0093-7314", "generic_name": "Clopidogrel", "labeler_name": "Teva Pharmaceuticals USA, 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"}