nafcillin
Generic: nafcillin sodium
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
nafcillin
Generic Name
nafcillin sodium
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
nafcillin sodium 1 g/4mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-327
Product ID
63323-327_89168d2d-2dc0-3f50-e053-2a95a90a31be
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090002
Listing Expiration
2026-12-31
Marketing Start
2011-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323327
Hyphenated Format
63323-327
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
ANDA090002 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/4mL
Packaging
- 10 VIAL in 1 CARTON (63323-327-10) / 4 mL in 1 VIAL (63323-327-21)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "89168d2d-2dc0-3f50-e053-2a95a90a31be", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721458", "1721460"], "spl_set_id": ["c39721a3-7b22-4720-9dbd-bc82f03d2af7"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-327-10) / 4 mL in 1 VIAL (63323-327-21)", "package_ndc": "63323-327-10", "marketing_start_date": "20110630"}], "brand_name": "Nafcillin", "product_id": "63323-327_89168d2d-2dc0-3f50-e053-2a95a90a31be", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "63323-327", "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": "1 g/4mL"}], "application_number": "ANDA090002", "marketing_category": "ANDA", "marketing_start_date": "20110630", "listing_expiration_date": "20261231"}