foscarnet sodium
Generic: foscarnet sodium
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
foscarnet sodium
Generic Name
foscarnet sodium
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
foscarnet sodium 24 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
23155-771
Product ID
23155-771_7de2fbfd-a1c3-4320-8212-bfeeff0a20a4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213807
Listing Expiration
2026-12-31
Marketing Start
2023-06-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155771
Hyphenated Format
23155-771
Supplemental Identifiers
RxCUI
UPC
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
ANDA213807 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 24 mg/mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (23155-771-31) / 250 mL in 1 BOTTLE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7de2fbfd-a1c3-4320-8212-bfeeff0a20a4", "openfda": {"upc": ["0323155771312"], "unii": ["964YS0OOG1"], "rxcui": ["1734377"], "spl_set_id": ["d2b4ce68-5a81-4b14-8914-21bc38f01008"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (23155-771-31) / 250 mL in 1 BOTTLE, GLASS", "package_ndc": "23155-771-31", "marketing_start_date": "20230605"}], "brand_name": "foscarnet sodium", "product_id": "23155-771_7de2fbfd-a1c3-4320-8212-bfeeff0a20a4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Chelating Activity [MoA]", "DNA Polymerase Inhibitors [MoA]", "Pyrophosphate Analog DNA Polymerase Inhibitor [EPC]", "Pyrophosphate Analog [EXT]"], "product_ndc": "23155-771", "generic_name": "foscarnet sodium", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "foscarnet sodium", "active_ingredients": [{"name": "FOSCARNET SODIUM", "strength": "24 mg/mL"}], "application_number": "ANDA213807", "marketing_category": "ANDA", "marketing_start_date": "20230605", "listing_expiration_date": "20261231"}