clopidogrel

Generic: clopidogrel bisulfate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 300 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-752
Product ID 68084-752_2c3a4450-fdb9-1ef8-e063-6294a90ab226
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076274
Listing Expiration 2026-12-31
Marketing Start 2014-03-28

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 68084752
Hyphenated Format 68084-752

Supplemental Identifiers

RxCUI
309362 749196
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 bisulfate (source: ndc)
Application Number ANDA076274 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (68084-752-19) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-18)
  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-752-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-95)
source: ndc

Packages (2)

Ingredients (1)

clopidogrel bisulfate (300 mg/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": "20 BLISTER PACK in 1 CARTON (68084-752-19)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-18)", "package_ndc": "68084-752-19", "marketing_start_date": "20230712"}, {"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-752-25)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-752-95)", "package_ndc": "68084-752-25", "marketing_start_date": "20140331"}], "brand_name": "Clopidogrel", "product_id": "68084-752_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": "68084-752", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "300 mg/1"}], "application_number": "ANDA076274", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}