nafcillin
Generic: nafcillin sodium
Labeler: avenacy inc.Drug Facts
Product Profile
Brand Name
nafcillin
Generic Name
nafcillin sodium
Labeler
avenacy inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
nafcillin sodium 10 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
83634-101
Product ID
83634-101_7a4b6e14-65c7-456d-999a-eb8dacaaeece
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090005
Listing Expiration
2026-12-31
Marketing Start
2025-02-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83634101
Hyphenated Format
83634-101
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 (83634-101-99) / 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": "7a4b6e14-65c7-456d-999a-eb8dacaaeece", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["0556378a-b794-4235-ba09-ebdc295e9092"], "manufacturer_name": ["Avenacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83634-101-99) / 100 mL in 1 BOTTLE", "package_ndc": "83634-101-99", "marketing_start_date": "20250201"}], "brand_name": "Nafcillin", "product_id": "83634-101_7a4b6e14-65c7-456d-999a-eb8dacaaeece", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "83634-101", "generic_name": "Nafcillin Sodium", "labeler_name": "Avenacy Inc.", "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": "20250201", "listing_expiration_date": "20261231"}