nafcillin
Generic: nafcillin
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
nafcillin
Generic Name
nafcillin
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
nafcillin sodium 2 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0338-1019
Product ID
0338-1019_ad3cc424-4e9f-49e8-b72b-6969ae6b16b8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA050655
Listing Expiration
2026-12-31
Marketing Start
1989-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03381019
Hyphenated Format
0338-1019
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
NDA050655 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/100mL
Packaging
- 100 mL in 1 BAG (0338-1019-48)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ad3cc424-4e9f-49e8-b72b-6969ae6b16b8", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721458", "1721460"], "spl_set_id": ["cd2d18c5-95a2-4fb4-bd8b-b5d39e2da416"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BAG (0338-1019-48)", "package_ndc": "0338-1019-48", "marketing_start_date": "19891031"}], "brand_name": "NAFCILLIN", "product_id": "0338-1019_ad3cc424-4e9f-49e8-b72b-6969ae6b16b8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "0338-1019", "generic_name": "NAFCILLIN", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAFCILLIN", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "2 g/100mL"}], "application_number": "NDA050655", "marketing_category": "NDA", "marketing_start_date": "19891031", "listing_expiration_date": "20261231"}