acyclovir

Generic: acyclovir

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acyclovir
Generic Name acyclovir
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acyclovir 800 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-228
Product ID 23155-228_6e0a075f-822f-457d-8ccc-e63a16746d76
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074891
Listing Expiration 2026-12-31
Marketing Start 2013-08-08

Pharmacologic Class

Established (EPC)
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]
Mechanism of Action
dna polymerase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155228
Hyphenated Format 23155-228

Supplemental Identifiers

RxCUI
197311 197313
UPC
0323155227017 0323155228014
UNII
X4HES1O11F
NUI
N0000020060 N0000180187 N0000180188 N0000175468 N0000175459

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name acyclovir (source: ndc)
Application Number ANDA074891 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-228-01)
  • 500 TABLET in 1 BOTTLE (23155-228-05)
source: ndc

Packages (2)

23155-228-01 100 TABLET in 1 BOTTLE (23155-228-01) 23155-228-05 500 TABLET in 1 BOTTLE (23155-228-05)

Ingredients (1)

acyclovir (800 mg/1)

Linked Drug Pages (1)

ACYCLOVIR ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e0a075f-822f-457d-8ccc-e63a16746d76", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000180188", "N0000175468", "N0000175459"], "upc": ["0323155227017", "0323155228014"], "unii": ["X4HES1O11F"], "rxcui": ["197311", "197313"], "spl_set_id": ["0de2f5c7-9e75-4bdf-9c28-e026cc6694b4"], "pharm_class_epc": ["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]"], "pharm_class_moa": ["DNA Polymerase Inhibitors [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-228-01)", "package_ndc": "23155-228-01", "marketing_start_date": "20130808"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-228-05)", "package_ndc": "23155-228-05", "marketing_start_date": "20130808"}], "brand_name": "ACYCLOVIR", "product_id": "23155-228_6e0a075f-822f-457d-8ccc-e63a16746d76", "dosage_form": "TABLET", "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": "23155-228", "generic_name": "ACYCLOVIR", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACYCLOVIR", "active_ingredients": [{"name": "ACYCLOVIR", "strength": "800 mg/1"}], "application_number": "ANDA074891", "marketing_category": "ANDA", "marketing_start_date": "20130808", "listing_expiration_date": "20261231"}