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United States · US · US:71205-388_32aa3f42-23a1-4867-8228-e6e76cf9f135
ACYCLOVIR
Orange BookUNIISPLATC J05AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeJ05AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11712053883030 TABLET in 1 BOTTLE (71205-388-30)
- ndc11712053883535 TABLET in 1 BOTTLE (71205-388-35)
- ndc11712053886060 TABLET in 1 BOTTLE (71205-388-60)
- ndc11712053889090 TABLET in 1 BOTTLE (71205-388-90)
Annotations
UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A074891
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": "71205-388_32aa3f42-23a1-4867-8228-e6e76cf9f135",
"productndc": "71205-388",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "074891",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Oct 31, 1997"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "002",
"approval_date": "Oct 31, 1997"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACYCLOVIR",
"proprietary_name": "ACYCLOVIR",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074891",
"marketing_category": "ANDA",
"nonproprietary_name": "ACYCLOVIR",
"start_marketing_date": "20130808",
"active_numerator_strength": "800"
}Related drugs
Other records sharing ATC code J05AB01.
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