acyclovir
Generic: acyclovir
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
acyclovir
Generic Name
acyclovir
Labeler
zydus lifesciences limited
Dosage Form
TABLET
Routes
Active Ingredients
acyclovir 800 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65841-803
Product ID
65841-803_b401b7c4-9c22-470f-981e-da74bef39dc6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204314
Listing Expiration
2026-12-31
Marketing Start
2014-09-10
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65841803
Hyphenated Format
65841-803
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA204314 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 800 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (65841-803-01)
- 500 TABLET in 1 BOTTLE (65841-803-05)
- 30 TABLET in 1 BOTTLE (65841-803-06)
- 1000 TABLET in 1 BOTTLE (65841-803-10)
- 90 TABLET in 1 BOTTLE (65841-803-16)
- 10 BLISTER PACK in 1 CARTON (65841-803-30) / 10 TABLET in 1 BLISTER PACK
Packages (6)
65841-803-01
100 TABLET in 1 BOTTLE (65841-803-01)
65841-803-05
500 TABLET in 1 BOTTLE (65841-803-05)
65841-803-06
30 TABLET in 1 BOTTLE (65841-803-06)
65841-803-10
1000 TABLET in 1 BOTTLE (65841-803-10)
65841-803-16
90 TABLET in 1 BOTTLE (65841-803-16)
65841-803-30
10 BLISTER PACK in 1 CARTON (65841-803-30) / 10 TABLET in 1 BLISTER PACK
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b401b7c4-9c22-470f-981e-da74bef39dc6", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000180188", "N0000175468", "N0000175459"], "upc": ["0365841803013"], "unii": ["X4HES1O11F"], "rxcui": ["197311", "197313"], "spl_set_id": ["8d9fea43-6c04-40d7-8aac-398c2de2a558"], "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": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65841-803-01)", "package_ndc": "65841-803-01", "marketing_start_date": "20140910"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65841-803-05)", "package_ndc": "65841-803-05", "marketing_start_date": "20140910"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65841-803-06)", "package_ndc": "65841-803-06", "marketing_start_date": "20140910"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-803-10)", "package_ndc": "65841-803-10", "marketing_start_date": "20140910"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65841-803-16)", "package_ndc": "65841-803-16", "marketing_start_date": "20140910"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-803-30) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "65841-803-30", "marketing_start_date": "20140910"}], "brand_name": "acyclovir", "product_id": "65841-803_b401b7c4-9c22-470f-981e-da74bef39dc6", "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": "65841-803", "generic_name": "acyclovir", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acyclovir", "active_ingredients": [{"name": "ACYCLOVIR", "strength": "800 mg/1"}], "application_number": "ANDA204314", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}