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United States · US · US:71335-0969_d1050818-e0b0-4be8-88c3-80e4a20e5250
Sildenafil
Orange BookUNIISPLATC G04BE03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG04BE03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc11713350969015 TABLET, FILM COATED in 1 BOTTLE (71335-0969-0)
- ndc11713350969110 TABLET, FILM COATED in 1 BOTTLE (71335-0969-1)
- ndc1171335096925 TABLET, FILM COATED in 1 BOTTLE (71335-0969-2)
- ndc11713350969330 TABLET, FILM COATED in 1 BOTTLE (71335-0969-3)
- ndc1171335096942 TABLET, FILM COATED in 1 BOTTLE (71335-0969-4)
- ndc1171335096956 TABLET, FILM COATED in 1 BOTTLE (71335-0969-5)
- ndc11713350969620 TABLET, FILM COATED in 1 BOTTLE (71335-0969-6)
- ndc1171335096974 TABLET, FILM COATED in 1 BOTTLE (71335-0969-7)
- ndc11713350969890 TABLET, FILM COATED in 1 BOTTLE (71335-0969-8)
- ndc11713350969960 TABLET, FILM COATED in 1 BOTTLE (71335-0969-9)
Annotations
UNII (FDA Substance ID)
BW9B0ZE037
SILDENAFIL CITRATE
RxCUI 221161
Orange Book
A202023
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "BW9B0ZE037",
"rxcui": "221161",
"inchikey": "DEIYFTQMQPDXOT-UHFFFAOYSA-N",
"display_name": "SILDENAFIL CITRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"78c4551c-b922-43c9-9a5a-66377ea07bc2": {
"match": "brand_token",
"title": "SILDENAFIL CITRATE (SILDENAFIL) TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
"spl_version": "24",
"published_date": "2026-05-29"
}
},
"productid": "71335-0969_d1050818-e0b0-4be8-88c3-80e4a20e5250",
"productndc": "71335-0969",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "202023",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 25MG BASE",
"product_no": "001",
"approval_date": "Jun 27, 2018"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 50MG BASE",
"product_no": "002",
"approval_date": "Jun 27, 2018"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 100MG BASE",
"product_no": "003",
"approval_date": "Jun 27, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SILDENAFIL CITRATE",
"proprietary_name": "Sildenafil",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202023",
"marketing_category": "ANDA",
"nonproprietary_name": "Sildenafil",
"start_marketing_date": "20180628",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code G04BE03.
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