NAFCILLIN SODIUM

Generic: NAFCILLIN SODIUM

Labeler: Steriscience Specialties Private Limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name NAFCILLIN SODIUM
Generic Name NAFCILLIN SODIUM
Labeler Steriscience Specialties Private Limited
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (82449-503-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

NAFCILLIN SODIUM (1 g/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"}