clopidogrel bisulfate

Generic: clopidogrel bisulfate

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

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7700
Product ID 68788-7700_470788b4-fbba-4d33-9fd2-ed3cb67064b0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204165
Listing Expiration 2026-12-31
Marketing Start 2020-05-01

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 687887700
Hyphenated Format 68788-7700

Supplemental Identifiers

RxCUI
309362
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 bisulfate (source: ndc)
Generic Name clopidogrel bisulfate (source: ndc)
Application Number ANDA204165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7700-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7700-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7700-9)
source: ndc

Packages (3)

68788-7700-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7700-3) 68788-7700-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7700-6) 68788-7700-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7700-9)

Ingredients (1)

clopidogrel bisulfate (75 mg/1)

Linked Drug Pages (1)

Clopidogrel bisulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "470788b4-fbba-4d33-9fd2-ed3cb67064b0", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["e51d4bcc-01df-409d-9179-45e6536ac25b"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7700-3)", "package_ndc": "68788-7700-3", "marketing_start_date": "20200501"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7700-6)", "package_ndc": "68788-7700-6", "marketing_start_date": "20200501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7700-9)", "package_ndc": "68788-7700-9", "marketing_start_date": "20200501"}], "brand_name": "Clopidogrel bisulfate", "product_id": "68788-7700_470788b4-fbba-4d33-9fd2-ed3cb67064b0", "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": "68788-7700", "generic_name": "Clopidogrel bisulfate", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel bisulfate", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA204165", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}