nafcillin
Generic: nafcillin sodium
Labeler: athenex pharmaceutical division, llc.Drug Facts
Product Profile
Brand Name
nafcillin
Generic Name
nafcillin sodium
Labeler
athenex pharmaceutical division, llc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
nafcillin sodium 10 g/100mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70860119
Hyphenated Format
70860-119
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 g/100mL
Packaging
- 1 BOTTLE in 1 CARTON (70860-119-99) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}