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United States · US · US:55150-155_410e306b-e8b9-4ff5-b703-a3005eec272f
Acyclovir Sodium
Orange BookUNIISPLATC J05AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEugia US LLC
CountryUS (United States)
ATC codeJ05AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11551501552010 VIAL, SINGLE-DOSE in 1 CARTON (55150-155-20) / 20 mL in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
927L42J563
ACYCLOVIR SODIUM
RxCUI 81944
Orange Book
A203701
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": "55150-155_410e306b-e8b9-4ff5-b703-a3005eec272f",
"productndc": "55150-155",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "203701",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 50MG BASE/ML",
"product_no": "001",
"approval_date": "Oct 11, 2013"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ACYCLOVIR SODIUM",
"proprietary_name": "Acyclovir Sodium",
"active_ingred_unit": "mg/20mL",
"application_number": "ANDA203701",
"marketing_category": "ANDA",
"nonproprietary_name": "Acyclovir Sodium",
"start_marketing_date": "20131011",
"active_numerator_strength": "1000"
}Related drugs
Other records sharing ATC code J05AB01.
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