60505-3992
Generic: clopidogrel bisulfate
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
Generic Name
clopidogrel bisulfate
Labeler
apotex corp.
Dosage Form
TABLET, FILM COATED
Active Ingredients
clopidogrel bisulfate 75 mg/1
Identifiers & Regulatory
Product NDC
60505-3992
Product ID
60505-3992_60d8badd-53dc-6631-e244-e5ebc5fce094
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2012-05-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605053992
Hyphenated Format
60505-3992
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: label)
Generic Name
clopidogrel bisulfate (source: ndc)
Application Number
ANDA076274 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 75 mg/1
Packaging
- 39000 TABLET, FILM COATED in 1 PAIL (60505-3992-8)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "60d8badd-53dc-6631-e244-e5ebc5fce094", "openfda": {}, "finished": false, "packaging": [{"description": "39000 TABLET, FILM COATED in 1 PAIL (60505-3992-8)", "package_ndc": "60505-3992-8", "marketing_start_date": "17-MAY-12"}], "product_id": "60505-3992_60d8badd-53dc-6631-e244-e5ebc5fce094", "dosage_form": "TABLET, FILM COATED", "product_ndc": "60505-3992", "generic_name": "clopidogrel bisulfate", "labeler_name": "Apotex Corp.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}