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United States · US · US:71335-1649_841b6c33-e16d-4bbb-80df-3c35c73287d3

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
    7133516490
    50 TABLET, FILM COATED in 1 BOTTLE (71335-1649-0)
  • ndc11
    7133516491
    10 TABLET, FILM COATED in 1 BOTTLE (71335-1649-1)
  • ndc11
    7133516492
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1649-2)
  • ndc11
    7133516493
    7 TABLET, FILM COATED in 1 BOTTLE (71335-1649-3)
  • ndc11
    7133516494
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1649-4)
  • ndc11
    7133516495
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1649-5)
  • ndc11
    7133516496
    20 TABLET, FILM COATED in 1 BOTTLE (71335-1649-6)
  • ndc11
    7133516497
    270 TABLET, FILM COATED in 1 BOTTLE (71335-1649-7)
  • ndc11
    7133516498
    15 TABLET, FILM COATED in 1 BOTTLE (71335-1649-8)
  • ndc11
    7133516499
    12 TABLET, FILM COATED in 1 BOTTLE (71335-1649-9)

Annotations

UNII (FDA Substance ID)
BW9B0ZE037
SILDENAFIL CITRATE
RxCUI 221161
Orange Book
A203623
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": "71335-1649_841b6c33-e16d-4bbb-80df-3c35c73287d3",
  "productndc": "71335-1649",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "203623",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Nov 26, 2014"
      }
    ],
    "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": "ANDA203623",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sildenafil",
  "start_marketing_date": "20141126",
  "active_numerator_strength": "20"
}

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