Package 70436-089-55
Brand: ganciclovir
Generic: ganciclovir sodiumPackage Facts
Identity
Package NDC
70436-089-55
Digits Only
7043608955
Product NDC
70436-089
Description
25 VIAL in 1 CARTON (70436-089-55) / 10 mL in 1 VIAL
Marketing
Marketing Status
Brand
ganciclovir
Generic
ganciclovir sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2c55a80a-e482-1d6b-e063-6394a90a41c4", "openfda": {"upc": ["0370436089550"], "unii": ["02L083W284"], "rxcui": ["310442"], "spl_set_id": ["eb100366-2a64-4742-af11-6177a8a494c8"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70436-089-55) / 10 mL in 1 VIAL", "package_ndc": "70436-089-55", "marketing_start_date": "20190101"}], "brand_name": "ganciclovir", "product_id": "70436-089_2c55a80a-e482-1d6b-e063-6394a90a41c4", "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": "70436-089", "generic_name": "ganciclovir sodium", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ganciclovir", "active_ingredients": [{"name": "GANCICLOVIR SODIUM", "strength": "500 mg/10mL"}], "application_number": "ANDA204204", "marketing_category": "ANDA", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}