Package 68001-641-41
Brand: enoxaparin sodium
Generic: enoxaparin sodiumPackage Facts
Identity
Package NDC
68001-641-41
Digits Only
6800164141
Product NDC
68001-641
Description
1 VIAL, MULTI-DOSE in 1 CARTON (68001-641-41) / 3 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
Brand
enoxaparin sodium
Generic
enoxaparin sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "3f6241ed-b5ff-9869-e063-6294a90a0156", "openfda": {"unii": ["8NZ41MIK1O"], "rxcui": ["854255"], "spl_set_id": ["d978e06e-b758-460b-81d3-69f7a5b89b00"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (68001-641-41) / 3 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "68001-641-41", "marketing_start_date": "20250501"}], "brand_name": "Enoxaparin Sodium", "product_id": "68001-641_3f6241ed-b5ff-9869-e063-6294a90a0156", "dosage_form": "INJECTION", "pharm_class": ["Heparin", "Low-Molecular-Weight [CS]", "Low Molecular Weight Heparin [EPC]"], "product_ndc": "68001-641", "generic_name": "Enoxaparin Sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enoxaparin Sodium", "active_ingredients": [{"name": "ENOXAPARIN SODIUM", "strength": "300 mg/3mL"}], "application_number": "ANDA214856", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}