clopidogrel

Generic: clopidogrel

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 16714-052
Product ID 16714-052_dbf6d86e-5d4f-40da-a933-b928843053b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202928
Listing Expiration 2026-12-31
Marketing Start 2022-08-09

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 16714052
Hyphenated Format 16714-052

Supplemental Identifiers

RxCUI
309362
UPC
0316714052045 0316714052038 0316714052014 0316714052021
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 (source: ndc)
Application Number ANDA202928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (16714-052-01)
  • 90 TABLET in 1 BOTTLE (16714-052-02)
  • 500 TABLET in 1 BOTTLE (16714-052-03)
  • 1000 TABLET in 1 BOTTLE (16714-052-04)
  • 10 TABLET in 1 BLISTER PACK (16714-052-10)
  • 100 TABLET in 1 BOX, UNIT-DOSE (16714-052-11)
source: ndc

Packages (6)

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": "dbf6d86e-5d4f-40da-a933-b928843053b7", "openfda": {"upc": ["0316714052045", "0316714052038", "0316714052014", "0316714052021"], "unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["d176de1d-b1b3-4aa9-b783-d53f65a79e50"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16714-052-01)", "package_ndc": "16714-052-01", "marketing_start_date": "20220809"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (16714-052-02)", "package_ndc": "16714-052-02", "marketing_start_date": "20220809"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16714-052-03)", "package_ndc": "16714-052-03", "marketing_start_date": "20220809"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16714-052-04)", "package_ndc": "16714-052-04", "marketing_start_date": "20230425"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (16714-052-10)", "package_ndc": "16714-052-10", "marketing_start_date": "20220809"}, {"sample": false, "description": "100 TABLET in 1 BOX, UNIT-DOSE (16714-052-11)", "package_ndc": "16714-052-11", "marketing_start_date": "20220809"}], "brand_name": "Clopidogrel", "product_id": "16714-052_dbf6d86e-5d4f-40da-a933-b928843053b7", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "16714-052", "generic_name": "Clopidogrel", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA202928", "marketing_category": "ANDA", "marketing_start_date": "20220809", "listing_expiration_date": "20261231"}