nafcillin

Generic: nafcillin sodium

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nafcillin
Generic Name nafcillin sodium
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

nafcillin sodium 10 g/100mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-198
Product ID 25021-198_f50e7f65-8bca-4df1-bff1-8069b33def90
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090005
Listing Expiration 2026-12-31
Marketing Start 2025-04-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021198
Hyphenated Format 25021-198

Supplemental Identifiers

RxCUI
239189
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 ANDA090005 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (25021-198-99) / 100 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

nafcillin sodium (10 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f50e7f65-8bca-4df1-bff1-8069b33def90", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["a6a4e122-b7f5-4eb5-8555-7aea6eda794b"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-198-99)  / 100 mL in 1 VIAL", "package_ndc": "25021-198-99", "marketing_start_date": "20250415"}], "brand_name": "Nafcillin", "product_id": "25021-198_f50e7f65-8bca-4df1-bff1-8069b33def90", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "25021-198", "generic_name": "Nafcillin Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nafcillin", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "10 g/100mL"}], "application_number": "ANDA090005", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}