clopidogrel

Generic: clopidogrel bisulfate

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-199
Product ID 72205-199_0b4edca9-12af-4534-baad-4fa5c1cc9ac8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215388
Listing Expiration 2026-12-31
Marketing Start 2024-09-20

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 72205199
Hyphenated Format 72205-199

Supplemental Identifiers

RxCUI
309362
UPC
0372205199057 0372205199309 0372205199903 0372205199019
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 (source: ndc)
Generic Name clopidogrel bisulfate (source: ndc)
Application Number ANDA215388 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72205-199-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (72205-199-05)
  • 10 BLISTER PACK in 1 CARTON (72205-199-06) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-199-11)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72205-199-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72205-199-90)
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": "0b4edca9-12af-4534-baad-4fa5c1cc9ac8", "openfda": {"upc": ["0372205199057", "0372205199309", "0372205199903", "0372205199019"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["1447a095-c663-4f05-91d4-f09bfc0c3d42"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72205-199-01)", "package_ndc": "72205-199-01", "marketing_start_date": "20251112"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72205-199-05)", "package_ndc": "72205-199-05", "marketing_start_date": "20241122"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72205-199-06)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-199-11)", "package_ndc": "72205-199-06", "marketing_start_date": "20241122"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72205-199-30)", "package_ndc": "72205-199-30", "marketing_start_date": "20241122"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72205-199-90)", "package_ndc": "72205-199-90", "marketing_start_date": "20241122"}], "brand_name": "CLOPIDOGREL", "product_id": "72205-199_0b4edca9-12af-4534-baad-4fa5c1cc9ac8", "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": "72205-199", "generic_name": "CLOPIDOGREL BISULFATE", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CLOPIDOGREL", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA215388", "marketing_category": "ANDA", "marketing_start_date": "20240920", "listing_expiration_date": "20261231"}