clopidogrel
Generic: clopidogrel bisulfate
Labeler: legacy pharmaceutical packaging, llcDrug Facts
Product Profile
Brand Name
clopidogrel
Generic Name
clopidogrel bisulfate
Labeler
legacy pharmaceutical packaging, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
clopidogrel bisulfate 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68645-590
Product ID
68645-590_4c21fe89-421c-249a-e063-6294a90aad2c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090540
Listing Expiration
2027-12-31
Marketing Start
2012-05-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68645590
Hyphenated Format
68645-590
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 90 TABLET, FILM COATED in 1 BOTTLE (68645-590-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c21fe89-421c-249a-e063-6294a90aad2c", "openfda": {"upc": ["0368645590905"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["53de10a5-dbd0-413d-90e5-00a1920ec391"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68645-590-90)", "package_ndc": "68645-590-90", "marketing_start_date": "20120517"}], "brand_name": "Clopidogrel", "product_id": "68645-590_4c21fe89-421c-249a-e063-6294a90aad2c", "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": "68645-590", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "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": "20271231"}