acyclovir sodium

Generic: acyclovir sodium

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acyclovir sodium
Generic Name acyclovir sodium
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

acyclovir sodium 1000 mg/20mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-155
Product ID 84549-155_3a390591-86f7-b68d-e063-6294a90a8bcc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203701
Listing Expiration 2026-12-31
Marketing Start 2013-10-11

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549155
Hyphenated Format 84549-155

Supplemental Identifiers

RxCUI
1734934
UNII
927L42J563

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 acyclovir sodium (source: ndc)
Generic Name acyclovir sodium (source: ndc)
Application Number ANDA203701 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1000 mg/20mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, SINGLE-DOSE (84549-155-20)
source: ndc

Packages (1)

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

Ingredients (1)

acyclovir sodium (1000 mg/20mL)

Linked Drug Pages (1)

Acyclovir Sodium ndc-match (0.9)

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"}