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United States · US · US:71335-9721_637f4303-bd11-4934-b45d-d353b402cffd
Acyclovir
Orange BookUNIISPLATC J05AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeJ05AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc117133597210500 TABLET in 1 BOTTLE, PLASTIC (71335-9721-0)
- ndc11713359721125 TABLET in 1 BOTTLE, PLASTIC (71335-9721-1)
- ndc11713359721235 TABLET in 1 BOTTLE, PLASTIC (71335-9721-2)
- ndc11713359721330 TABLET in 1 BOTTLE, PLASTIC (71335-9721-3)
- ndc11713359721460 TABLET in 1 BOTTLE, PLASTIC (71335-9721-4)
- ndc11713359721550 TABLET in 1 BOTTLE, PLASTIC (71335-9721-5)
- ndc11713359721610 TABLET in 1 BOTTLE, PLASTIC (71335-9721-6)
- ndc11713359721740 TABLET in 1 BOTTLE, PLASTIC (71335-9721-7)
- ndc11713359721821 TABLET in 1 BOTTLE, PLASTIC (71335-9721-8)
- ndc11713359721990 TABLET in 1 BOTTLE, PLASTIC (71335-9721-9)
Annotations
UNII (FDA Substance ID)
X4HES1O11F
ACYCLOVIR
RxCUI 281
Orange Book
A075382
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": "71335-9721_637f4303-bd11-4934-b45d-d353b402cffd",
"productndc": "71335-9721",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075382",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "400MG",
"product_no": "001",
"approval_date": "Apr 30, 1999"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "002",
"approval_date": "Apr 30, 1999"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACYCLOVIR",
"proprietary_name": "Acyclovir",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075382",
"marketing_category": "ANDA",
"nonproprietary_name": "Acyclovir",
"start_marketing_date": "20091022",
"active_numerator_strength": "800"
}Related drugs
Other records sharing ATC code J05AB01.
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