oxacillin
Generic: oxacillin
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
oxacillin
Generic Name
oxacillin
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
oxacillin sodium 1 g/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-813
Product ID
63323-813_c7907a70-1efa-46eb-b046-fcf043fdb413
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206198
Listing Expiration
2026-12-31
Marketing Start
2020-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323813
Hyphenated Format
63323-813
Supplemental Identifiers
RxCUI
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
oxacillin (source: ndc)
Generic Name
oxacillin (source: ndc)
Application Number
ANDA206198 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/20mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (63323-813-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-813-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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 (63323-813-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-813-01)", "package_ndc": "63323-813-20", "marketing_start_date": "20201101"}], "brand_name": "Oxacillin", "product_id": "63323-813_c7907a70-1efa-46eb-b046-fcf043fdb413", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63323-813", "generic_name": "Oxacillin", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxacillin", "active_ingredients": [{"name": "OXACILLIN SODIUM", "strength": "1 g/20mL"}], "application_number": "ANDA206198", "marketing_category": "ANDA", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}