Sildenafil Citrate

Product NDC
50436-3500
11-digit product format
504363500
Labeler code
50436
Product ID
50436-3500_09e9dc1f-ec21-4f46-b322-9ae222aee44b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sildenafil citrate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Unit Dose Services
Application
NDA020895
Marketing category
NDA
Marketing start
2017-12-01
Marketing end
0000-00-00
Substance
SILDENAFIL CITRATE
Active strength
50 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fabccea2-36c8-9268-ee44-ec231455538fProduct name920241217
ac996ae9-22a2-41c2-bb86-913c4aef95adProduct name120230606
fc95c9f0-00dc-40ef-bcea-b60c9009c5fcProduct name920220613

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50436-3500-1Sildenafil Citrate1080 in 1 CASETABLET, FILM COATED10802
50436-3500-1Sildenafil Citrate1 in 1 POUCHTABLET, FILM COATED12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50436-3500SILDENAFIL CITRATE TABLET, FILM COATED [UNIT DOSE SERVICES]2Legacy NDC, 2 package rows20191120_7a4c81f9-826b-4d36-adc9-e6d8a839845e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312950sildenafil citrate 50 MG Oral TabletPSN7a4c81f9-826b-4d36-adc9-e6d8a839845e2
312950sildenafil 50 MG Oral TabletSCD7a4c81f9-826b-4d36-adc9-e6d8a839845e2
312950sildenafil 50 MG (as sildenafil citrate) Oral TabletSY7a4c81f9-826b-4d36-adc9-e6d8a839845e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
50436-3500-1504363500011080 in 1 CASEHistorical