NDC 71335-1437

Sildenafil Citrate

Sildenafil

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

Product ID71335-1437_5c72f066-b07e-4c79-b1c2-cb36a0c4bd76
NDC71335-1437
Product TypeHuman Prescription Drug
Proprietary NameSildenafil Citrate
Generic NameSildenafil
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-10-12
Marketing CategoryANDA / ANDA
Application NumberANDA206401
Labeler NameBryant Ranch Prepack
Substance NameSILDENAFIL CITRATE
Active Ingredient Strength100 mg/1
Pharm ClassesPhosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71335-1437-0

15 TABLET, FILM COATED in 1 BOTTLE (71335-1437-0)
Marketing Start Date2019-12-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1437-7 [71335143707]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-3 [71335143703]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-5 [71335143705]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-4 [71335143704]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-6 [71335143706]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-9 [71335143709]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-8 [71335143708]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-0 [71335143700]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-2 [71335143702]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 71335-1437-1 [71335143701]

Sildenafil Citrate TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA206401
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

Drug Details

Active Ingredients

IngredientStrength
SILDENAFIL CITRATE100 mg/1

Pharmacological Class

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

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

NDCBrand NameGeneric Name
0904-6671SILDENAFIL CITRATESILDENAFIL CITRATE
13668-185SILDENAFIL CITRATESILDENAFIL CITRATE
13668-186Sildenafil CitrateSildenafil
70518-1641Sildenafil CitrateSildenafil Citrate
71205-231Sildenafil CitrateSildenafil Citrate
13668-188SILDENAFIL CITRATESILDENAFIL CITRATE
13668-187SILDENAFIL CITRATESILDENAFIL CITRATE
27241-069Sildenafil CitrateSildenafil Citrate
27241-068Sildenafil CitrateSildenafil Citrate
27241-067Sildenafil CitrateSildenafil Citrate
42543-005Sildenafil CitrateSildenafil Citrate
43063-941Sildenafil CitrateSildenafil Citrate
43063-940Sildenafil CitrateSildenafil Citrate
45865-937Sildenafil CitrateSildenafil Citrate
50090-3495Sildenafil CitrateSildenafil Citrate
50090-3493Sildenafil CitrateSildenafil Citrate
50090-3905SILDENAFIL CITRATESILDENAFIL CITRATE
50090-3494Sildenafil CitrateSildenafil Citrate
50436-0295Sildenafil CitrateSildenafil Citrate
50436-0035Sildenafil CitrateSildenafil Citrate
50436-0005Sildenafil CitrateSildenafil Citrate
50436-0185SILDENAFIL CITRATESILDENAFIL CITRATE
52817-295Sildenafil CitrateSildenafil Citrate
59762-0035Sildenafil CitrateSildenafil Citrate
59762-0034Sildenafil CitrateSildenafil Citrate
59762-0036Sildenafil CitrateSildenafil Citrate
68071-4854Sildenafil CitrateSildenafil Citrate
17856-8100Sildenafil CitrateSildenafil Citrate
68071-4744Sildenafil CitrateSildenafil Citrate
70934-421Sildenafil CitrateSildenafil Citrate
71205-305Sildenafil CitrateSildenafil Citrate
73160-005sildenafil citratesildenafil citrate
50436-0036Sildenafil CitrateSildenafil Citrate
50436-3500Sildenafil CitrateSildenafil Citrate
67877-648Sildenafil CitrateSildenafil Citrate
70934-435Sildenafil CitrateSildenafil Citrate
0069-0336Revatiosildenafil citrate
0069-0338Revatiosildenafil citrate
0069-4190Revatiosildenafil citrate
0093-5341SildenafilSildenafil
0093-5342SildenafilSildenafil
0093-5343SildenafilSildenafil
0093-5517SildenafilSildenafil
0179-0160Sildenafilsildenafil citrate
0378-1658Sildenafilsildenafil
0378-1659Sildenafilsildenafil
0378-1660Sildenafilsildenafil
0591-4050SildenafilSildenafil
0069-4200Viagrasildenafil citrate
0069-4210Viagrasildenafil citrate
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