oxacillin

Generic: oxacillin

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxacillin
Generic Name oxacillin
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

oxacillin sodium 2 g/50mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-1015
Product ID 0338-1015_dc761dcc-7333-4b1c-90be-e9ec96e7b2aa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050640
Listing Expiration 2026-12-31
Marketing Start 1989-10-26

Pharmacologic Class

Classes
penicillin-class antibacterial [epc] penicillins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03381015
Hyphenated Format 0338-1015

Supplemental Identifiers

RxCUI
240637 312128
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 NDA050640 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/50mL
source: ndc
Packaging
  • 50 mL in 1 BAG (0338-1015-41)
source: ndc

Packages (1)

Ingredients (1)

oxacillin sodium (2 g/50mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "dc761dcc-7333-4b1c-90be-e9ec96e7b2aa", "openfda": {"unii": ["G0V6C994Q5"], "rxcui": ["240637", "312128"], "spl_set_id": ["d893e45b-7f18-4c67-b10c-1e2e52a6b3ef"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BAG (0338-1015-41)", "package_ndc": "0338-1015-41", "marketing_start_date": "19891026"}], "brand_name": "OXACILLIN", "product_id": "0338-1015_dc761dcc-7333-4b1c-90be-e9ec96e7b2aa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0338-1015", "generic_name": "OXACILLIN", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXACILLIN", "active_ingredients": [{"name": "OXACILLIN SODIUM", "strength": "2 g/50mL"}], "application_number": "NDA050640", "marketing_category": "NDA", "marketing_start_date": "19891026", "listing_expiration_date": "20261231"}