acyclovir
Generic: acyclovir
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
acyclovir
Generic Name
acyclovir
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
acyclovir 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3250
Product ID
50090-3250_0c61c8ca-1f35-4ffa-b0a1-888b08f47f5f
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
500903250
Hyphenated Format
50090-3250
Supplemental Identifiers
RxCUI
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
ANDA204314 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 2 TABLET in 1 BOTTLE (50090-3250-0)
- 25 TABLET in 1 BOTTLE (50090-3250-2)
- 50 TABLET in 1 BOTTLE (50090-3250-3)
- 15 TABLET in 1 BOTTLE (50090-3250-4)
- 30 TABLET in 1 BOTTLE (50090-3250-5)
- 60 TABLET in 1 BOTTLE (50090-3250-6)
- 45 TABLET in 1 BOTTLE (50090-3250-9)
Packages (7)
50090-3250-0
2 TABLET in 1 BOTTLE (50090-3250-0)
50090-3250-2
25 TABLET in 1 BOTTLE (50090-3250-2)
50090-3250-3
50 TABLET in 1 BOTTLE (50090-3250-3)
50090-3250-4
15 TABLET in 1 BOTTLE (50090-3250-4)
50090-3250-5
30 TABLET in 1 BOTTLE (50090-3250-5)
50090-3250-6
60 TABLET in 1 BOTTLE (50090-3250-6)
50090-3250-9
45 TABLET in 1 BOTTLE (50090-3250-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c61c8ca-1f35-4ffa-b0a1-888b08f47f5f", "openfda": {"nui": ["N0000020060", "N0000180187", "N0000180188", "N0000175468", "N0000175459"], "unii": ["X4HES1O11F"], "rxcui": ["197311"], "spl_set_id": ["c40a57b9-4cf1-4a69-abf3-eb99a7fcda00"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (50090-3250-0)", "package_ndc": "50090-3250-0", "marketing_start_date": "20181015"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE (50090-3250-2)", "package_ndc": "50090-3250-2", "marketing_start_date": "20171108"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (50090-3250-3)", "package_ndc": "50090-3250-3", "marketing_start_date": "20171108"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-3250-4)", "package_ndc": "50090-3250-4", "marketing_start_date": "20171108"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-3250-5)", "package_ndc": "50090-3250-5", "marketing_start_date": "20171108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-3250-6)", "package_ndc": "50090-3250-6", "marketing_start_date": "20171108"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (50090-3250-9)", "package_ndc": "50090-3250-9", "marketing_start_date": "20171108"}], "brand_name": "acyclovir", "product_id": "50090-3250_0c61c8ca-1f35-4ffa-b0a1-888b08f47f5f", "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": "50090-3250", "generic_name": "acyclovir", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "acyclovir", "active_ingredients": [{"name": "ACYCLOVIR", "strength": "400 mg/1"}], "application_number": "ANDA204314", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}