acyclovir
Generic: acyclovir
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
acyclovir
Generic Name
acyclovir
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
acyclovir 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2447
Product ID
68071-2447_2048c55f-8391-e891-e063-6394a90a06fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075382
Listing Expiration
2026-12-31
Marketing Start
2009-10-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680712447
Hyphenated Format
68071-2447
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA075382 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 21 TABLET in 1 BOTTLE, PLASTIC (68071-2447-1)
- 30 TABLET in 1 BOTTLE, PLASTIC (68071-2447-3)
- 40 TABLET in 1 BOTTLE, PLASTIC (68071-2447-4)
- 25 TABLET in 1 BOTTLE, PLASTIC (68071-2447-5)
- 60 TABLET in 1 BOTTLE, PLASTIC (68071-2447-6)
- 15 TABLET in 1 BOTTLE, PLASTIC (68071-2447-8)
Packages (6)
68071-2447-1
21 TABLET in 1 BOTTLE, PLASTIC (68071-2447-1)
68071-2447-3
30 TABLET in 1 BOTTLE, PLASTIC (68071-2447-3)
68071-2447-4
40 TABLET in 1 BOTTLE, PLASTIC (68071-2447-4)
68071-2447-5
25 TABLET in 1 BOTTLE, PLASTIC (68071-2447-5)
68071-2447-6
60 TABLET in 1 BOTTLE, PLASTIC (68071-2447-6)
68071-2447-8
15 TABLET in 1 BOTTLE, PLASTIC (68071-2447-8)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2048c55f-8391-e891-e063-6394a90a06fb", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000180188", "N0000175468", "N0000175459"], "upc": ["0368071244786"], "unii": ["X4HES1O11F"], "rxcui": ["197311"], "spl_set_id": ["c46d5033-b1b2-e213-e053-2995a90ae6a3"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (68071-2447-1)", "package_ndc": "68071-2447-1", "marketing_start_date": "20210610"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-2447-3)", "package_ndc": "68071-2447-3", "marketing_start_date": "20210610"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (68071-2447-4)", "package_ndc": "68071-2447-4", "marketing_start_date": "20210610"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE, PLASTIC (68071-2447-5)", "package_ndc": "68071-2447-5", "marketing_start_date": "20210610"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (68071-2447-6)", "package_ndc": "68071-2447-6", "marketing_start_date": "20210610"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (68071-2447-8)", "package_ndc": "68071-2447-8", "marketing_start_date": "20210610"}], "brand_name": "Acyclovir", "product_id": "68071-2447_2048c55f-8391-e891-e063-6394a90a06fb", "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": "68071-2447", "generic_name": "Acyclovir", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acyclovir", "active_ingredients": [{"name": "ACYCLOVIR", "strength": "400 mg/1"}], "application_number": "ANDA075382", "marketing_category": "ANDA", "marketing_start_date": "20091022", "listing_expiration_date": "20261231"}