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United States · US · US:63629-5029_9b2a355b-6ad7-44e7-97a0-9cc736fa479e

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

  • ndc11
    6362950290
    50 TABLET in 1 BOTTLE (63629-5029-0)
  • ndc11
    6362950291
    10 TABLET in 1 BOTTLE (63629-5029-1)
  • ndc11
    6362950292
    30 TABLET in 1 BOTTLE (63629-5029-2)
  • ndc11
    6362950293
    7 TABLET in 1 BOTTLE (63629-5029-3)
  • ndc11
    6362950294
    90 TABLET in 1 BOTTLE (63629-5029-4)
  • ndc11
    6362950295
    60 TABLET in 1 BOTTLE (63629-5029-5)
  • ndc11
    6362950296
    20 TABLET in 1 BOTTLE (63629-5029-6)
  • ndc11
    6362950297
    270 TABLET in 1 BOTTLE (63629-5029-7)
  • ndc11
    6362950298
    15 TABLET in 1 BOTTLE (63629-5029-8)
  • ndc11
    6362950299
    12 TABLET in 1 BOTTLE (63629-5029-9)

Annotations

UNII (FDA Substance ID)
BW9B0ZE037
SILDENAFIL CITRATE
RxCUI 221161
Orange Book
A202025
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": "63629-5029_9b2a355b-6ad7-44e7-97a0-9cc736fa479e",
  "productndc": "63629-5029",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202025",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Feb 28, 2013"
      }
    ],
    "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": "ANDA202025",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sildenafil",
  "start_marketing_date": "20121108",
  "active_numerator_strength": "20"
}

Related drugs

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