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United States · US · US:71335-2657_b8d4e426-c062-4c2d-89ca-9bd8d13da405

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
    7133526570
    50 TABLET, FILM COATED in 1 BOTTLE (71335-2657-0)
  • ndc11
    7133526571
    10 TABLET, FILM COATED in 1 BOTTLE (71335-2657-1)
  • ndc11
    7133526572
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2657-2)
  • ndc11
    7133526573
    7 TABLET, FILM COATED in 1 BOTTLE (71335-2657-3)
  • ndc11
    7133526574
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2657-4)
  • ndc11
    7133526575
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2657-5)
  • ndc11
    7133526576
    20 TABLET, FILM COATED in 1 BOTTLE (71335-2657-6)
  • ndc11
    7133526577
    270 TABLET, FILM COATED in 1 BOTTLE (71335-2657-7)
  • ndc11
    7133526578
    15 TABLET, FILM COATED in 1 BOTTLE (71335-2657-8)
  • ndc11
    7133526579
    12 TABLET, FILM COATED in 1 BOTTLE (71335-2657-9)

Annotations

UNII (FDA Substance ID)
BW9B0ZE037
SILDENAFIL CITRATE
RxCUI 221161
Orange Book
A091479
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": "71335-2657_b8d4e426-c062-4c2d-89ca-9bd8d13da405",
  "productndc": "71335-2657",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "091479",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 20MG BASE",
        "product_no": "001",
        "approval_date": "Nov 6, 2012"
      }
    ],
    "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": "ANDA091479",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Sildenafil",
  "start_marketing_date": "20121106",
  "active_numerator_strength": "20"
}

Related drugs

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