clopidogrel
Generic: clopidogrel bisulfate
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
clopidogrel
Generic Name
clopidogrel bisulfate
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
clopidogrel bisulfate 75 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-536
Product ID
68084-536_2c3a4450-fdb9-1ef8-e063-6294a90ab226
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076274
Listing Expiration
2026-12-31
Marketing Start
2014-04-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084536
Hyphenated Format
68084-536
Supplemental Identifiers
RxCUI
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
ANDA076274 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-536-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-536-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c3a4450-fdb9-1ef8-e063-6294a90ab226", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362", "749196"], "spl_set_id": ["65ea4dc6-acb2-4609-9a4c-4866ef0ccb11"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-536-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-536-11)", "package_ndc": "68084-536-01", "marketing_start_date": "20140424"}], "brand_name": "Clopidogrel", "product_id": "68084-536_2c3a4450-fdb9-1ef8-e063-6294a90ab226", "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": "68084-536", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA076274", "marketing_category": "ANDA", "marketing_start_date": "20140424", "listing_expiration_date": "20261231"}