clopidogrel bisulfate

Generic: clopidogrel bisulfate

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

Drug Facts

Product Profile

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

clopidogrel bisulfate 75 mg/1

Manufacturer
RADHA PHARMACEUTICALS, INC.

Identifiers & Regulatory

Product NDC 77771-124
Product ID 77771-124_09ac9273-240e-b149-e063-6394a90a20cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204165
Listing Expiration 2026-12-31
Marketing Start 2023-02-20

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 77771124
Hyphenated Format 77771-124

Supplemental Identifiers

RxCUI
309362 749196
UPC
0377771124908 0377771124106 0377771124304
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 ANDA204165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (77771-124-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (77771-124-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (77771-124-90)
source: ndc

Packages (3)

77771-124-10 1000 TABLET, FILM COATED in 1 BOTTLE (77771-124-10) 77771-124-30 30 TABLET, FILM COATED in 1 BOTTLE (77771-124-30) 77771-124-90 90 TABLET, FILM COATED in 1 BOTTLE (77771-124-90)

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": "09ac9273-240e-b149-e063-6394a90a20cb", "openfda": {"upc": ["0377771124908", "0377771124106", "0377771124304"], "unii": ["08I79HTP27"], "rxcui": ["309362", "749196"], "spl_set_id": ["16aef4f6-6b90-4d5f-9e07-c9927adf3841"], "manufacturer_name": ["RADHA PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (77771-124-10)", "package_ndc": "77771-124-10", "marketing_start_date": "20230220"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (77771-124-30)", "package_ndc": "77771-124-30", "marketing_start_date": "20230220"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (77771-124-90)", "package_ndc": "77771-124-90", "marketing_start_date": "20230220"}], "brand_name": "Clopidogrel bisulfate", "product_id": "77771-124_09ac9273-240e-b149-e063-6394a90a20cb", "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": "77771-124", "generic_name": "Clopidogrel bisulfate", "labeler_name": "RADHA 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": "20230220", "listing_expiration_date": "20261231"}