clopidogrel bisulfate

Generic: clopidogrel bisulfate

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

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-5277
Product ID 68071-5277_1d7904db-ccb2-b88e-e063-6294a90ac568
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204165
Listing Expiration 2026-12-31
Marketing Start 2015-09-15

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 680715277
Hyphenated Format 68071-5277

Supplemental Identifiers

RxCUI
309362
UPC
0368071527797
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
  • 90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)
source: ndc

Packages (1)

Ingredients (1)

clopidogrel bisulfate (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d7904db-ccb2-b88e-e063-6294a90ac568", "openfda": {"upc": ["0368071527797"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["a7bf847d-43e9-166e-e053-2995a90a239e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)", "package_ndc": "68071-5277-9", "marketing_start_date": "20200610"}], "brand_name": "Clopidogrel bisulfate", "product_id": "68071-5277_1d7904db-ccb2-b88e-e063-6294a90ac568", "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": "68071-5277", "generic_name": "Clopidogrel bisulfate", "labeler_name": "NuCare 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": "20150915", "listing_expiration_date": "20261231"}