clopidogrel
Generic: clopidogrel
Labeler: northstar rxllcDrug Facts
Product Profile
Brand Name
clopidogrel
Generic Name
clopidogrel
Labeler
northstar rxllc
Dosage Form
TABLET
Routes
Active Ingredients
clopidogrel bisulfate 75 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714052
Hyphenated Format
16714-052
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 75 mg/1
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)
Packages (6)
16714-052-01
30 TABLET in 1 BOTTLE (16714-052-01)
16714-052-02
90 TABLET in 1 BOTTLE (16714-052-02)
16714-052-03
500 TABLET in 1 BOTTLE (16714-052-03)
16714-052-04
1000 TABLET in 1 BOTTLE (16714-052-04)
16714-052-10
10 TABLET in 1 BLISTER PACK (16714-052-10)
16714-052-11
100 TABLET in 1 BOX, UNIT-DOSE (16714-052-11)
Ingredients (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"}