Sildenafil

Product NDC
71610-271
11-digit product format
716100271
Labeler code
71610
Product ID
71610-271_35c2453d-fbb5-4101-9e04-bd47131d3ada
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sildenafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA077342
Marketing category
ANDA
Marketing start
2018-05-29
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71610-271SILDENAFIL TABLET, FILM COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]1Legacy NDC20190515_7fa82ca0-3e75-4424-918b-520678975ca5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71610-271-02716100271022 TABLET, FILM COATED in 1 BOTTLE (71610-271-02) 2019-05-010000-00-00NoNoCurrent
71610-271-04716100271044 TABLET, FILM COATED in 1 BOTTLE (71610-271-04) 2019-05-010000-00-00NoNoCurrent
71610-271-06716100271066 TABLET, FILM COATED in 1 BOTTLE (71610-271-06) 2019-05-010000-00-00NoNoCurrent
71610-271-127161002711212 TABLET, FILM COATED in 1 BOTTLE (71610-271-12) 2019-05-010000-00-00NoNoCurrent