foscarnet sodium
Generic: foscarnet sodium
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
foscarnet sodium
Generic Name
foscarnet sodium
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
foscarnet sodium 6000 mg/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
43066-089
Product ID
43066-089_f3b7e70d-5ed4-4d9a-a11b-84c3c4deb607
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213001
Listing Expiration
2027-12-31
Marketing Start
2023-08-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43066089
Hyphenated Format
43066-089
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
foscarnet sodium (source: ndc)
Generic Name
foscarnet sodium (source: ndc)
Application Number
ANDA213001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6000 mg/250mL
Packaging
- 10 BAG in 1 CARTON (43066-089-10) / 250 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f3b7e70d-5ed4-4d9a-a11b-84c3c4deb607", "openfda": {"unii": ["964YS0OOG1"], "rxcui": ["1734377"], "spl_set_id": ["8a7caffd-9d8a-4d45-ad48-70d511a89c29"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CARTON (43066-089-10) / 250 mL in 1 BAG", "package_ndc": "43066-089-10", "marketing_start_date": "20230828"}], "brand_name": "FOSCARNET SODIUM", "product_id": "43066-089_f3b7e70d-5ed4-4d9a-a11b-84c3c4deb607", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Chelating Activity [MoA]", "DNA Polymerase Inhibitors [MoA]", "Pyrophosphate Analog DNA Polymerase Inhibitor [EPC]", "Pyrophosphate Analog [EXT]"], "product_ndc": "43066-089", "generic_name": "foscarnet sodium", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FOSCARNET SODIUM", "active_ingredients": [{"name": "FOSCARNET SODIUM", "strength": "6000 mg/250mL"}], "application_number": "ANDA213001", "marketing_category": "ANDA", "marketing_start_date": "20230828", "listing_expiration_date": "20271231"}