Sildenafil

Product NDC
50090-4646
11-digit product format
500904646
Labeler code
50090
Product ID
50090-4646_b324fb5c-e007-4b24-84d9-609f8f43abf1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sildenafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202023
Marketing category
ANDA
Marketing start
2018-06-28
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
2022-12-31
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
50090-4646-0Sildenafil10 in 1 BOTTLETABLET, FILM COATED104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-4646SILDENAFIL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]4Legacy NDC, 1 package rows20210417_69361f7c-daef-4b17-9ee8-48e818df4dbb.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312950sildenafil citrate 50 MG Oral TabletPSN69361f7c-daef-4b17-9ee8-48e818df4dbb4
312950sildenafil 50 MG Oral TabletSCD69361f7c-daef-4b17-9ee8-48e818df4dbb4
312950sildenafil 50 MG (as sildenafil citrate) Oral TabletSY69361f7c-daef-4b17-9ee8-48e818df4dbb4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-4646-05009046460010 TABLET, FILM COATED in 1 BOTTLE (50090-4646-0) 2019-10-240000-00-00NoNoCurrent