NAFCILLIN SODIUM
Generic: NAFCILLIN SODIUM
Labeler: Steriscience Specialties Private LimitedDrug Facts
Product Profile
Brand Name
NAFCILLIN SODIUM
Generic Name
NAFCILLIN SODIUM
Labeler
Steriscience Specialties Private Limited
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
NAFCILLIN SODIUM 1 g/1
Identifiers & Regulatory
Product NDC
82449-503
Product ID
82449-503_07e8b20a-f473-78ed-e063-6394a90a3340
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200002
Listing Expiration
2026-12-31
Marketing Start
2023-10-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82449503
Hyphenated Format
82449-503
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 SODIUM (source: ndc)
Generic Name
NAFCILLIN SODIUM (source: ndc)
Application Number
ANDA200002 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL in 1 CARTON (82449-503-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "07e8b20a-f473-78ed-e063-6394a90a3340", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721458", "1721460"], "spl_set_id": ["344455bd-051d-4c4a-b76e-8c4dd9351d97"], "manufacturer_name": ["Steriscience Specialties Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (82449-503-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "82449-503-02", "marketing_start_date": "20231017"}], "brand_name": "NAFCILLIN SODIUM", "product_id": "82449-503_07e8b20a-f473-78ed-e063-6394a90a3340", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "82449-503", "generic_name": "NAFCILLIN SODIUM", "labeler_name": "Steriscience Specialties Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAFCILLIN SODIUM", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA200002", "marketing_category": "ANDA", "marketing_start_date": "20231017", "listing_expiration_date": "20261231"}