acyclovir

Generic: acyclovir

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acyclovir
Generic Name acyclovir
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acyclovir 400 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-856
Product ID 60687-856_4a03039d-ae31-10ea-e063-6294a90a1e30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074891
Listing Expiration 2027-12-31
Marketing Start 2025-03-24

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 60687856
Hyphenated Format 60687-856

Supplemental Identifiers

RxCUI
197311 197313
UNII
X4HES1O11F
NUI
N0000020060 N0000180187 N0000180188 N0000175468 N0000175459

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
  • 400 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (60687-856-01) / 1 TABLET in 1 BLISTER PACK (60687-856-11)
  • 50 BLISTER PACK in 1 CARTON (60687-856-65) / 1 TABLET in 1 BLISTER PACK (60687-856-11)
source: ndc

Packages (2)

60687-856-01 100 BLISTER PACK in 1 CARTON (60687-856-01) / 1 TABLET in 1 BLISTER PACK (60687-856-11) 60687-856-65 50 BLISTER PACK in 1 CARTON (60687-856-65) / 1 TABLET in 1 BLISTER PACK (60687-856-11)

Ingredients (1)

acyclovir (400 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": "4a03039d-ae31-10ea-e063-6294a90a1e30", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000180188", "N0000175468", "N0000175459"], "unii": ["X4HES1O11F"], "rxcui": ["197311", "197313"], "spl_set_id": ["05f42300-2a06-45f1-a9b9-6e5c84ae58ec"], "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": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-856-01)  / 1 TABLET in 1 BLISTER PACK (60687-856-11)", "package_ndc": "60687-856-01", "marketing_start_date": "20250324"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (60687-856-65)  / 1 TABLET in 1 BLISTER PACK (60687-856-11)", "package_ndc": "60687-856-65", "marketing_start_date": "20260204"}], "brand_name": "ACYCLOVIR", "product_id": "60687-856_4a03039d-ae31-10ea-e063-6294a90a1e30", "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": "60687-856", "generic_name": "ACYCLOVIR", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACYCLOVIR", "active_ingredients": [{"name": "ACYCLOVIR", "strength": "400 mg/1"}], "application_number": "ANDA074891", "marketing_category": "ANDA", "marketing_start_date": "20250324", "listing_expiration_date": "20271231"}