nafcillin

Generic: nafcillin sodium

Labeler: athenex pharmaceutical division, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nafcillin
Generic Name nafcillin sodium
Labeler athenex pharmaceutical division, llc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

nafcillin sodium 10 g/100mL

Manufacturer
Athenex Pharmaceutical Division, LLC.

Identifiers & Regulatory

Product NDC 70860-119
Product ID 70860-119_2cc9cc61-54ac-9a94-e063-6394a90a2376
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090005
Marketing Start 2018-08-15
Marketing End 2026-06-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70860119
Hyphenated Format 70860-119

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 BOTTLE in 1 CARTON (70860-119-99) / 100 mL in 1 BOTTLE
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": "2cc9cc61-54ac-9a94-e063-6394a90a2376", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["2bc91eeb-5d8d-4058-b16a-532ba114fcd5"], "manufacturer_name": ["Athenex Pharmaceutical Division, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70860-119-99)  / 100 mL in 1 BOTTLE", "package_ndc": "70860-119-99", "marketing_end_date": "20260630", "marketing_start_date": "20180815"}], "brand_name": "Nafcillin", "product_id": "70860-119_2cc9cc61-54ac-9a94-e063-6394a90a2376", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70860-119", "generic_name": "nafcillin sodium", "labeler_name": "Athenex Pharmaceutical Division, LLC.", "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_end_date": "20260630", "marketing_start_date": "20180815"}