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United States · US · US:0074-2340_389fa9db-7528-4d2a-9518-8909d396177b
Norvir
Orange BookUNIISPLATC J05AE03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbbVie Inc.
CountryUS (United States)
ATC codeJ05AE03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11007423403030 TABLET, FILM COATED in 1 BOTTLE (0074-2340-30)
Annotations
UNII (FDA Substance ID)
O3J8G9O825
RITONAVIR
RxCUI 85762
Orange Book
N022417
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "O3J8G9O825",
"rxcui": "85762",
"inchikey": "NCDNCNXCDXHOMX-XGKFQTDJSA-N",
"display_name": "RITONAVIR",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"2849298e-de6e-47bb-8194-56e075b33fc3": {
"match": "brand_token",
"title": "NORVIR (RITONAVIR) TABLET, FILM COATED NORVIR (RITONAVIR) SOLUTION NORVIR (RITONAVIR) POWDER [ABBVIE INC.]",
"spl_version": "1651",
"published_date": "2025-11-21"
}
},
"productid": "0074-2340_389fa9db-7528-4d2a-9518-8909d396177b",
"productndc": "0074-2340",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "022417",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "100MG",
"product_no": "001",
"approval_date": "Feb 10, 2010"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RITONAVIR",
"proprietary_name": "Norvir",
"active_ingred_unit": "mg/1",
"application_number": "NDA022417",
"marketing_category": "NDA",
"nonproprietary_name": "Ritonavir",
"start_marketing_date": "20220816",
"active_numerator_strength": "100"
}Related drugs
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