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United States · US · US:50090-7202_40466844-1948-49fd-abef-f4d0629c07bd
Tenofovir Disoproxil Fumarate
Orange BookUNIISPLATC J05AF07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeJ05AF07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11500907202030 TABLET, FILM COATED in 1 BOTTLE (50090-7202-0)
Annotations
UNII (FDA Substance ID)
OTT9J7900I
TENOFOVIR DISOPROXIL FUMARATE
RxCUI 322248
Orange Book
A090636
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "OTT9J7900I",
"rxcui": "322248",
"inchikey": "VCMJCVGFSROFHV-WZGZYPNHSA-N",
"display_name": "TENOFOVIR DISOPROXIL FUMARATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"7f0bc342-0a0a-1d28-e053-2991aa0a28b9": {
"match": "brand_token",
"title": "TENOFOVIR DISOPROXIL FUMARATE TABLET, FILM COATED [AVKARE]",
"spl_version": "5",
"published_date": "2026-01-16"
}
},
"productid": "50090-7202_40466844-1948-49fd-abef-f4d0629c07bd",
"productndc": "50090-7202",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "090636",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "300MG",
"product_no": "001",
"approval_date": "Jan 26, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TENOFOVIR DISOPROXIL FUMARATE",
"proprietary_name": "Tenofovir Disoproxil Fumarate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA090636",
"marketing_category": "ANDA",
"nonproprietary_name": "Tenofovir Disoproxil Fumarate",
"start_marketing_date": "20181112",
"active_numerator_strength": "300"
}Related drugs
Other records sharing ATC code J05AF07.
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