NDC 50436-1210

Sildenafil

Sildenafil

Sildenafil is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Unit Dose Services. The primary component is Sildenafil Citrate.

Product ID50436-1210_00ae7c9e-960a-407a-a705-e5b708a7d026
NDC50436-1210
Product TypeHuman Prescription Drug
Proprietary NameSildenafil
Generic NameSildenafil
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2014-01-03
Marketing CategoryANDA / ANDA
Application NumberANDA203814
Labeler NameUnit Dose Services
Substance NameSILDENAFIL CITRATE
Active Ingredient Strength20 mg/1
Pharm ClassesPhosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 50436-1210-1

250 POUCH in 1 CASE (50436-1210-1) > 3 TABLET, FILM COATED in 1 POUCH
Marketing Start Date2018-04-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50436-1210-4 [50436121004]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-08-01

NDC 50436-1210-5 [50436121005]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-11-13

NDC 50436-1210-6 [50436121006]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-11-13

NDC 50436-1210-1 [50436121001]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-04

NDC 50436-1210-3 [50436121003]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-08-01

NDC 50436-1210-2 [50436121002]

Sildenafil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203814
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-08-01

Drug Details

Active Ingredients

IngredientStrength
SILDENAFIL CITRATE20 mg/1

OpenFDA Data

SPL SET ID:b812890c-41a1-4f72-a06a-b550a0ca034e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 577033

    • Pharmacological Class

    • Phosphodiesterase 5 Inhibitor [EPC]
    • Phosphodiesterase 5 Inhibitors [MoA]
    • Phosphodiesterase 5 Inhibitor [EPC]
    • Phosphodiesterase 5 Inhibitors [MoA]

    NDC Crossover Matching brand name "Sildenafil" or generic name "Sildenafil"

    NDCBrand NameGeneric Name
    0093-5341SildenafilSildenafil
    0093-5342SildenafilSildenafil
    0093-5343SildenafilSildenafil
    0093-5517SildenafilSildenafil
    0179-0160Sildenafilsildenafil citrate
    0378-1657Sildenafilsildinafil
    0378-1658Sildenafilsildenafil
    0378-1659Sildenafilsildenafil
    0378-1660Sildenafilsildenafil
    0591-4050SildenafilSildenafil
    68001-176SildenafilSildenafil
    68001-363SildenafilSildenafil
    68071-2072SildenafilSildenafil
    68071-1979SildenafilSildenafil
    68071-1687SildenafilSildenafil
    68071-3137SildenafilSildenafil
    68071-3329SildenafilSildenafil
    68071-4517SildenafilSildenafil
    68071-4599SildenafilSildenafil
    68071-4617SildenafilSildenafil
    68071-4674SildenafilSildenafil
    68084-869SildenafilSildenafil
    68788-7379SildenafilSildenafil
    68788-7218SildenafilSildenafil
    70518-0438SildenafilSildenafil
    70518-1216SildenafilSildenafil
    70518-1844SildenafilSildenafil
    70859-015SildenafilSildenafil
    71205-088SildenafilSildenafil
    71205-220SildenafilSildenafil
    71335-0969SildenafilSildenafil
    71335-1005SildenafilSildenafil
    71335-0288SildenafilSildenafil
    71335-1028SildenafilSildenafil
    71610-237SildenafilSildenafil
    76519-1135SildenafilSildenafil
    76519-1216SILDENAFILSILDENAFIL
    76519-1218SILDENAFILSILDENAFIL
    27241-124SildenafilSildenafil
    31722-710SildenafilSildenafil
    31722-776SildenafilSildenafil
    31722-711SildenafilSildenafil
    31722-709SildenafilSildenafil
    33342-121SildenafilSildenafil
    42291-747SildenafilSildenafil
    42291-748SildenafilSildenafil
    42291-746SildenafilSildenafil
    42291-749SildenafilSildenafil
    43063-668SildenafilSildenafil
    43063-550SildenafilSildenafil
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.