Package 0955-1016-01

Brand: enoxaparin sodium

Generic: enoxaparin sodium
NDC Package

Package Facts

Identity

Package NDC 0955-1016-01
Digits Only 0955101601
Product NDC 0955-1016
Description

1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01) / 3 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2011-10-03
Brand enoxaparin sodium
Generic enoxaparin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "48bacfb7-7152-45b1-a188-59c4a205f5b0", "openfda": {"unii": ["8NZ41MIK1O"], "rxcui": ["854228", "854235", "854238", "854241", "854245", "854248", "854252", "854255"], "spl_set_id": ["20635579-c92d-4f6c-a332-1096d51002f2"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0955-1016-01)  / 3 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0955-1016-01", "marketing_start_date": "20111003"}], "brand_name": "Enoxaparin sodium", "product_id": "0955-1016_48bacfb7-7152-45b1-a188-59c4a205f5b0", "dosage_form": "INJECTION", "pharm_class": ["Heparin", "Low-Molecular-Weight [CS]", "Low Molecular Weight Heparin [EPC]"], "product_ndc": "0955-1016", "generic_name": "enoxaparin sodium", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enoxaparin sodium", "active_ingredients": [{"name": "ENOXAPARIN SODIUM", "strength": "300 mg/3mL"}], "application_number": "NDA020164", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20111003", "listing_expiration_date": "20271231"}