ganciclovir
Generic: ganciclovir sodium
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ganciclovir
Generic Name
ganciclovir sodium
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
ganciclovir sodium 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9299
Product ID
0143-9299_192fd7cc-3a38-4afe-82f3-a4d89238b1ad
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076222
Listing Expiration
2026-12-31
Marketing Start
2021-06-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439299
Hyphenated Format
0143-9299
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
ganciclovir (source: ndc)
Generic Name
ganciclovir sodium (source: ndc)
Application Number
ANDA076222 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 10 VIAL in 1 BOX (0143-9299-10) / 10 mL in 1 VIAL (0143-9299-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "192fd7cc-3a38-4afe-82f3-a4d89238b1ad", "openfda": {"unii": ["02L083W284"], "rxcui": ["310442"], "spl_set_id": ["4f8219ca-6780-4131-8962-9c3fdd0a84dd"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (0143-9299-10) / 10 mL in 1 VIAL (0143-9299-01)", "package_ndc": "0143-9299-10", "marketing_start_date": "20210617"}], "brand_name": "Ganciclovir", "product_id": "0143-9299_192fd7cc-3a38-4afe-82f3-a4d89238b1ad", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "DNA Polymerase Inhibitors [MoA]", "Nucleoside Analog Antiviral [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "0143-9299", "generic_name": "Ganciclovir sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ganciclovir", "active_ingredients": [{"name": "GANCICLOVIR SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA076222", "marketing_category": "ANDA", "marketing_start_date": "20210617", "listing_expiration_date": "20261231"}