SILDENAFIL CITRATE

Product NDC
50090-7181
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SILDENAFIL CITRATE
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA209302
Marketing category
ANDA
Substance
SILDENAFIL CITRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7181-010 TABLET in 1 BOTTLE (50090-7181-0) 2024-06-10NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SILDENAFIL CITRATEA-S Medication Solutions2024-06-18HUMAN PRESCRIPTION DRUG LABEL1