clopidogrel

Generic: clopidogrel bisulfate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1898
Product ID 70518-1898_4987afa4-e527-4ae3-e063-6394a90aa694
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090540
Listing Expiration 2027-12-31
Marketing Start 2019-02-22

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 705181898
Hyphenated Format 70518-1898

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 (source: ndc)
Generic Name clopidogrel bisulfate (source: ndc)
Application Number ANDA090540 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1898-0)
source: ndc

Packages (1)

70518-1898-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1898-0)

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": "4987afa4-e527-4ae3-e063-6394a90aa694", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["3e2539c1-a6ad-4d60-944c-c2e7aa70ce45"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1898-0)", "package_ndc": "70518-1898-0", "marketing_start_date": "20190222"}], "brand_name": "Clopidogrel", "product_id": "70518-1898_4987afa4-e527-4ae3-e063-6394a90aa694", "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": "70518-1898", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "REMEDYREPACK INC.", "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": "20190222", "listing_expiration_date": "20271231"}