tadalafil

Product NDC
71335-2467
11-digit product format
713352467
Labeler code
71335
Product ID
71335-2467_f79b51c1-60c1-4a52-939e-81ee8f2148ae
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tadalafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA209250
Marketing category
ANDA
Marketing start
2019-03-26
Substance
TADALAFIL
Active strength
5 mg/1
Pharmacologic classes
Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
742SXX0ICTTADALAFIL171596-29-5TADALAFIL

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2467-17133524670130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-1) 2024-08-16NoNoHistorical
71335-2467-27133524670290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-2) 2024-08-16NoNoHistorical
71335-2467-37133524670315 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-3) 2024-08-16NoNoHistorical
71335-2467-47133524670460 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2467-4) 2024-08-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
tadalafilBryant Ranch Prepack2024-08-16HUMAN PRESCRIPTION DRUG LABEL1