Package 63323-812-20

Brand: oxacillin

Generic: oxacillin
NDC Package

Package Facts

Identity

Package NDC 63323-812-20
Digits Only 6332381220
Product NDC 63323-812
Product ID 63323-812_c7907a70-1efa-46eb-b046-fcf043fdb413
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (63323-812-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-812-01)

Marketing

Marketing Status
Marketed Since 2020-11-01
Brand oxacillin
Generic oxacillin
Sample Package No

Linked Drug Pages (1)

Oxacillin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "c7907a70-1efa-46eb-b046-fcf043fdb413", "openfda": {"unii": ["G0V6C994Q5"], "rxcui": ["1743547", "1743549"], "spl_set_id": ["af2dccac-98c8-488f-a133-6374b3ca8dba"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (63323-812-20)  / 20 mL in 1 VIAL, SINGLE-DOSE (63323-812-01)", "package_ndc": "63323-812-20", "marketing_start_date": "20201101"}], "brand_name": "Oxacillin", "product_id": "63323-812_c7907a70-1efa-46eb-b046-fcf043fdb413", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63323-812", "generic_name": "Oxacillin", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxacillin", "active_ingredients": [{"name": "OXACILLIN SODIUM", "strength": "2 g/20mL"}], "application_number": "ANDA206198", "marketing_category": "ANDA", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}