Package 84549-155-20

Brand: acyclovir sodium

Generic: acyclovir sodium
NDC Package

Package Facts

Identity

Package NDC 84549-155-20
Digits Only 8454915520
Product NDC 84549-155
Description

20 mL in 1 VIAL, SINGLE-DOSE (84549-155-20)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand acyclovir sodium
Generic acyclovir sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3a390591-86f7-b68d-e063-6294a90a8bcc", "openfda": {"unii": ["927L42J563"], "rxcui": ["1734934"], "spl_set_id": ["23a7cf9e-f21b-06c2-e063-6394a90aa623"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (84549-155-20)", "package_ndc": "84549-155-20", "marketing_start_date": "20250827"}], "brand_name": "Acyclovir Sodium", "product_id": "84549-155_3a390591-86f7-b68d-e063-6294a90a8bcc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["DNA Polymerase Inhibitors [MoA]", "Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]", "Nucleoside Analog [EXT]"], "product_ndc": "84549-155", "generic_name": "Acyclovir Sodium", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acyclovir Sodium", "active_ingredients": [{"name": "ACYCLOVIR SODIUM", "strength": "1000 mg/20mL"}], "application_number": "ANDA203701", "marketing_category": "ANDA", "marketing_start_date": "20131011", "listing_expiration_date": "20261231"}