nafcillin

Generic: nafcillin

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

Drug Facts

Product Profile

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

nafcillin sodium 2 g/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-1019
Product ID 0338-1019_ad3cc424-4e9f-49e8-b72b-6969ae6b16b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050655
Listing Expiration 2026-12-31
Marketing Start 1989-10-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03381019
Hyphenated Format 0338-1019

Supplemental Identifiers

RxCUI
1721458 1721460
UNII
49G3001BCK

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 nafcillin (source: ndc)
Generic Name nafcillin (source: ndc)
Application Number NDA050655 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/100mL
source: ndc
Packaging
  • 100 mL in 1 BAG (0338-1019-48)
source: ndc

Packages (1)

Ingredients (1)

nafcillin sodium (2 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ad3cc424-4e9f-49e8-b72b-6969ae6b16b8", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721458", "1721460"], "spl_set_id": ["cd2d18c5-95a2-4fb4-bd8b-b5d39e2da416"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BAG (0338-1019-48)", "package_ndc": "0338-1019-48", "marketing_start_date": "19891031"}], "brand_name": "NAFCILLIN", "product_id": "0338-1019_ad3cc424-4e9f-49e8-b72b-6969ae6b16b8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0338-1019", "generic_name": "NAFCILLIN", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAFCILLIN", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "2 g/100mL"}], "application_number": "NDA050655", "marketing_category": "NDA", "marketing_start_date": "19891031", "listing_expiration_date": "20261231"}