Package 42023-173-25

Brand: ganciclovir

Generic: ganciclovir
NDC Package

Package Facts

Identity

Package NDC 42023-173-25
Digits Only 4202317325
Product NDC 42023-173
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (42023-173-25) / 10 mL in 1 VIAL, SINGLE-DOSE (42023-173-01)

Marketing

Marketing Status
Marketed Since 2016-12-06
Brand ganciclovir
Generic ganciclovir
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f04cdda8-4829-4fa1-8cf2-503479c89b1e", "openfda": {"unii": ["02L083W284"], "rxcui": ["310442"], "spl_set_id": ["87afd103-6e64-444f-971d-0e732e9ae995"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (42023-173-25)  / 10 mL in 1 VIAL, SINGLE-DOSE (42023-173-01)", "package_ndc": "42023-173-25", "marketing_start_date": "20161206"}], "brand_name": "Ganciclovir", "product_id": "42023-173_f04cdda8-4829-4fa1-8cf2-503479c89b1e", "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": "42023-173", "generic_name": "Ganciclovir", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ganciclovir", "active_ingredients": [{"name": "GANCICLOVIR SODIUM", "strength": "500 mg/10mL"}], "application_number": "ANDA204950", "marketing_category": "ANDA", "marketing_start_date": "20161206", "listing_expiration_date": "20261231"}