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United States · US · US:72542-500_7720f74d-f161-4aaa-a421-7bf48e6c962c
OLPRUVA
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAcer Therapeutics Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11725425001890 BOX in 1 CARTON (72542-500-18) / 1 KIT in 1 BOX (72542-500-02) * 1 FOR SUSPENSION in 1 PACKET (72542-003-01) * 1 FOR SUSPENSION in 1 PACKET (72542-000-01) * 1 FOR SUSPENSION in 1 PACKET (72542-002-01)
Annotations
Orange Book
N214860
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "ORAL",
"spl_meta": {
"89abc31c-43e8-4809-9eb7-172cb31a86f1": {
"match": "brand_token",
"title": "OLPRUVA (SODIUM PHENYLBUTYRATE) KIT [ACER THERAPEUTICS INC.]",
"spl_version": "4",
"published_date": "2024-12-20"
}
},
"productid": "72542-500_7720f74d-f161-4aaa-a421-7bf48e6c962c",
"productndc": "72542-500",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "214860",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "2GM/PACKET",
"product_no": "001",
"approval_date": "Dec 22, 2022"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "3GM/PACKET",
"product_no": "002",
"approval_date": "Dec 22, 2022"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "4GM/PACKET",
"product_no": "003",
"approval_date": "Dec 22, 2022"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "5GM/PACKET",
"product_no": "004",
"approval_date": "Dec 22, 2022"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "6GM/PACKET",
"product_no": "005",
"approval_date": "Dec 22, 2022"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "6.67GM/PACKET",
"product_no": "006",
"approval_date": "Dec 22, 2022"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "0.5GM/PACKET",
"product_no": "007",
"approval_date": "Oct 10, 2025"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "1GM/PACKET",
"product_no": "008",
"approval_date": "Oct 10, 2025"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "OLPRUVA",
"active_ingred_unit": null,
"application_number": "NDA214860",
"marketing_category": "NDA",
"nonproprietary_name": "sodium phenylbutyrate",
"start_marketing_date": "20221222",
"active_numerator_strength": null
}Access this data programmatically
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