nafcillin

Generic: nafcillin sodium

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

Drug Facts

Product Profile

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

nafcillin sodium 2 g/8mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-328
Product ID 63323-328_89a714ea-e764-6aeb-e053-2995a90a8a89
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090002
Listing Expiration 2026-12-31
Marketing Start 2011-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323328
Hyphenated Format 63323-328

Supplemental Identifiers

RxCUI
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 sodium (source: ndc)
Application Number ANDA090002 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/8mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (63323-328-22) / 8 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

nafcillin sodium (2 g/8mL)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "89a714ea-e764-6aeb-e053-2995a90a8a89", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721460"], "spl_set_id": ["3c2581a1-8051-4d7a-a1f7-521248648dc9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-328-22)  / 8 mL in 1 VIAL", "package_ndc": "63323-328-22", "marketing_start_date": "20110630"}], "brand_name": "Nafcillin", "product_id": "63323-328_89a714ea-e764-6aeb-e053-2995a90a8a89", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63323-328", "generic_name": "Nafcillin Sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nafcillin", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "2 g/8mL"}], "application_number": "ANDA090002", "marketing_category": "ANDA", "marketing_start_date": "20110630", "listing_expiration_date": "20261231"}