foscarnet sodium

Generic: foscarnet sodium

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name foscarnet sodium
Generic Name foscarnet sodium
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

foscarnet sodium 6000 mg/250mL

Manufacturer
Baxter Healthcare Corporation

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
chelating activity [moa] dna polymerase inhibitors [moa] pyrophosphate analog dna polymerase inhibitor [epc] pyrophosphate analog [ext]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43066089
Hyphenated Format 43066-089

Supplemental Identifiers

RxCUI
1734377
UNII
964YS0OOG1

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 6000 mg/250mL
source: ndc
Packaging
  • 10 BAG in 1 CARTON (43066-089-10) / 250 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

foscarnet sodium (6000 mg/250mL)

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"}