clopidogrel

Generic: clopidogrel

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel
Labeler macleods pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-060
Product ID 33342-060_05355b6d-3802-4542-bda2-cd6a17e57266
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202928
Listing Expiration 2026-12-31
Marketing Start 2012-10-16

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 33342060
Hyphenated Format 33342-060

Supplemental Identifiers

RxCUI
309362
UPC
0333342060440 0333342060075 0333342060105
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 ANDA202928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (33342-060-07)
  • 90 TABLET in 1 BOTTLE (33342-060-10)
  • 100 TABLET in 1 BOX, UNIT-DOSE (33342-060-12)
  • 500 TABLET in 1 BOTTLE (33342-060-15)
  • 1000 TABLET in 1 BOTTLE (33342-060-44)
source: ndc

Packages (5)

33342-060-07 30 TABLET in 1 BOTTLE (33342-060-07) 33342-060-10 90 TABLET in 1 BOTTLE (33342-060-10) 33342-060-12 100 TABLET in 1 BOX, UNIT-DOSE (33342-060-12) 33342-060-15 500 TABLET in 1 BOTTLE (33342-060-15) 33342-060-44 1000 TABLET in 1 BOTTLE (33342-060-44)

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": "05355b6d-3802-4542-bda2-cd6a17e57266", "openfda": {"upc": ["0333342060440", "0333342060075", "0333342060105"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["063cd1eb-98fd-422e-8145-bba04c497efe"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (33342-060-07)", "package_ndc": "33342-060-07", "marketing_start_date": "20121016"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (33342-060-10)", "package_ndc": "33342-060-10", "marketing_start_date": "20140911"}, {"sample": false, "description": "100 TABLET in 1 BOX, UNIT-DOSE (33342-060-12)", "package_ndc": "33342-060-12", "marketing_start_date": "20121016"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (33342-060-15)", "package_ndc": "33342-060-15", "marketing_start_date": "20121016"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (33342-060-44)", "package_ndc": "33342-060-44", "marketing_start_date": "20230512"}], "brand_name": "Clopidogrel", "product_id": "33342-060_05355b6d-3802-4542-bda2-cd6a17e57266", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "33342-060", "generic_name": "Clopidogrel", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA202928", "marketing_category": "ANDA", "marketing_start_date": "20121016", "listing_expiration_date": "20261231"}