oxacillin

Generic: oxacillin

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxacillin
Generic Name oxacillin
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

oxacillin sodium 2 g/20mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-812
Product ID 63323-812_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
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323812
Hyphenated Format 63323-812

Supplemental Identifiers

RxCUI
1743547 1743549
UNII
G0V6C994Q5

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/20mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (63323-812-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-812-01)
source: ndc

Packages (1)

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

Ingredients (1)

oxacillin sodium (2 g/20mL)

Linked Drug Pages (1)

Oxacillin ndc-match (0.9)

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"}