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United States · US · US:76420-050_b01ced44-7b5d-5716-e053-2995a90a1263
acyclovir
Orange BookUNIISPLATC J05AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeJ05AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11764200501515 TABLET in 1 BOTTLE (76420-050-15)
- ndc11764200503030 TABLET in 1 BOTTLE (76420-050-30)
- ndc11764200506060 TABLET in 1 BOTTLE (76420-050-60)
Annotations
UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A077309
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "X4HES1O11F",
"rxcui": "281",
"inchikey": "MKUXAQIIEYXACX-UHFFFAOYSA-N",
"display_name": "ACYCLOVIR",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"db0a0ce5-dc39-4bd3-8b97-21ce9c9999f0": {
"match": "brand_token",
"title": "ACYCLOVIR TABLET [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "19",
"published_date": "2026-05-28"
}
},
"productid": "76420-050_b01ced44-7b5d-5716-e053-2995a90a1263",
"productndc": "76420-050",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "077309",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Sep 29, 2005"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "002",
"approval_date": "Sep 29, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACYCLOVIR",
"proprietary_name": "acyclovir",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077309",
"marketing_category": "ANDA",
"nonproprietary_name": "acyclovir",
"start_marketing_date": "20070609",
"active_numerator_strength": "400"
}Related drugs
Other records sharing ATC code J05AB01.
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