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United States · US · US:71205-391_51052f0e-1a07-405a-a962-981ce9439e02
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
- ndc11712053912525 TABLET in 1 BOTTLE (71205-391-25)
- ndc11712053913030 TABLET in 1 BOTTLE (71205-391-30)
- ndc11712053916060 TABLET in 1 BOTTLE (71205-391-60)
- ndc11712053919090 TABLET in 1 BOTTLE (71205-391-90)
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": "71205-391_51052f0e-1a07-405a-a962-981ce9439e02",
"productndc": "71205-391",
"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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