clopidogrel bisulfate

Generic: clopidogrel bisulfate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-894
Product ID 47335-894_2de2d0fb-68e7-4a22-8da8-be7658468f15
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090494
Listing Expiration 2026-12-31
Marketing Start 2012-05-18

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 47335894
Hyphenated Format 47335-894

Supplemental Identifiers

RxCUI
309362
UPC
0347335894813
UNII
08I79HTP27

Packaging Origin

Original Packager
true

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 ANDA090494 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (47335-894-13)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (47335-894-18)
  • 90 TABLET, FILM COATED in 1 BOTTLE (47335-894-19)
  • 90 TABLET, FILM COATED in 1 BOTTLE (47335-894-81)
  • 30 TABLET, FILM COATED in 1 BOTTLE (47335-894-83)
source: ndc

Packages (5)

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": "2de2d0fb-68e7-4a22-8da8-be7658468f15", "openfda": {"upc": ["0347335894813"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["d37db064-3a5a-4a0c-a60b-b4b417fe742a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (47335-894-13)", "package_ndc": "47335-894-13", "marketing_start_date": "20120518"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-894-18)", "package_ndc": "47335-894-18", "marketing_start_date": "20120518"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (47335-894-19)", "package_ndc": "47335-894-19", "marketing_start_date": "20120518"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (47335-894-81)", "package_ndc": "47335-894-81", "marketing_start_date": "20120518"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-894-83)", "package_ndc": "47335-894-83", "marketing_start_date": "20120518"}], "brand_name": "Clopidogrel Bisulfate", "product_id": "47335-894_2de2d0fb-68e7-4a22-8da8-be7658468f15", "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": "47335-894", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel Bisulfate", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA090494", "marketing_category": "ANDA", "marketing_start_date": "20120518", "listing_expiration_date": "20261231"}