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United States · US · US:71205-623_ad418ee5-a646-4d79-b10b-c7f3051f2977
Sildenafil Citrate
Orange BookUNIISPLATC G04BE03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerProficient Rx LP
CountryUS (United States)
ATC codeG04BE03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11712056231010 TABLET, FILM COATED in 1 BOTTLE (71205-623-10)
- ndc11712056233030 TABLET, FILM COATED in 1 BOTTLE (71205-623-30)
- ndc11712056236060 TABLET, FILM COATED in 1 BOTTLE (71205-623-60)
- ndc11712056239090 TABLET, FILM COATED in 1 BOTTLE (71205-623-90)
Annotations
UNII (FDA Substance ID)
BW9B0ZE037
SILDENAFIL CITRATE
RxCUI 221161
Orange Book
A204883
AB
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": "71205-623_ad418ee5-a646-4d79-b10b-c7f3051f2977",
"productndc": "71205-623",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "204883",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 20MG BASE",
"product_no": "001",
"approval_date": "Jun 20, 2016"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SILDENAFIL CITRATE",
"proprietary_name": "Sildenafil Citrate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204883",
"marketing_category": "ANDA",
"nonproprietary_name": "Sildenafil",
"start_marketing_date": "20160801",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code G04BE03.
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