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United States · US · US:63323-325_fc30a93e-1fe1-478d-bf68-fe8ab2575279
Acyclovir
Orange BookUNIISPLATC J05AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerFresenius Kabi USA, LLC
CountryUS (United States)
ATC codeJ05AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11633233251010 VIAL, SINGLE-DOSE in 1 TRAY (63323-325-10) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-325-03)
- ndc11633233252010 VIAL, SINGLE-DOSE in 1 TRAY (63323-325-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-325-09)
Annotations
UNII (FDA Substance ID)
927L42J563
ACYCLOVIR SODIUM
RxCUI 81944
Orange Book
A074930
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "927L42J563",
"rxcui": "81944",
"inchikey": "RMLUKZWYIKEASN-UHFFFAOYSA-M",
"display_name": "ACYCLOVIR SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"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": "63323-325_fc30a93e-1fe1-478d-bf68-fe8ab2575279",
"productndc": "63323-325",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "074930",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "EQ 50MG BASE/ML",
"product_no": "001",
"approval_date": "May 13, 1998"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACYCLOVIR SODIUM",
"proprietary_name": "Acyclovir",
"active_ingred_unit": "mg/mL",
"application_number": "ANDA074930",
"marketing_category": "ANDA",
"nonproprietary_name": "Acyclovir",
"start_marketing_date": "20001017",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code J05AB01.
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