Package 64380-153-01

Brand: valganciclovir

Generic: valganciclovir hydrochloride
NDC Package

Package Facts

Identity

Package NDC 64380-153-01
Digits Only 6438015301
Product NDC 64380-153
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-153-01)

Marketing

Marketing Status
Marketed Since 2022-09-12
Brand valganciclovir
Generic valganciclovir hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7b815816-a0ba-42d0-ba80-02894fa91b4b", "openfda": {"unii": ["4P3T9QF9NZ"], "rxcui": ["313566"], "spl_set_id": ["390691b2-3db0-4b9f-934f-120674726f14"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-153-01)", "package_ndc": "64380-153-01", "marketing_start_date": "20220912"}], "brand_name": "Valganciclovir", "product_id": "64380-153_7b815816-a0ba-42d0-ba80-02894fa91b4b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "DNA Polymerase Inhibitors [MoA]", "Nucleoside Analog Antiviral [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "64380-153", "generic_name": "Valganciclovir hydrochloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valganciclovir", "active_ingredients": [{"name": "VALGANCICLOVIR HYDROCHLORIDE", "strength": "450 mg/1"}], "application_number": "ANDA200790", "marketing_category": "ANDA", "marketing_start_date": "20220912", "listing_expiration_date": "20261231"}