nafcillin
Generic: nafcillin
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
nafcillin
Generic Name
nafcillin
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
nafcillin sodium 10 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-330
Product ID
63323-330_8b27ca5e-a933-7606-e053-2a95a90a0a33
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090005
Listing Expiration
2026-12-31
Marketing Start
2011-04-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323330
Hyphenated Format
63323-330
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 (source: ndc)
Application Number
ANDA090005 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/100mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-330-60) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8b27ca5e-a933-7606-e053-2a95a90a0a33", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["bbf0d8e4-b8e4-4958-b6b6-f0b9960f3b6a"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-330-60) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "63323-330-60", "marketing_start_date": "20110427"}], "brand_name": "Nafcillin", "product_id": "63323-330_8b27ca5e-a933-7606-e053-2a95a90a0a33", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63323-330", "generic_name": "NAFCILLIN", "labeler_name": "Fresenius Kabi USA, 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_start_date": "20110427", "listing_expiration_date": "20261231"}