Sildenafil Citrate

Product NDC
50090-3494
11-digit product format
500903494
Labeler code
50090
Product ID
50090-3494_cb1243ed-e267-4b82-b2fa-3d53c4f281fe
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sildenafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA091448
Marketing category
ANDA
Marketing start
2017-12-11
Marketing end
0000-00-00
Substance
SILDENAFIL CITRATE
Active strength
25 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-3494-02021-05-06C16284748780-19d75b9d0-526c-f424-e053-dadaa90a57ce81256b7b-a897-453f-88fc-0b7b417b6487
50090-3494-02020-01-31C16284748780-19d75b9d0-526c-f424-e053-dadaa90a57ce81256b7b-a897-453f-88fc-0b7b417b6487