Cialis

Product NDC
63629-7145
11-digit product format
636297145
Labeler code
63629
Product ID
63629-7145_aeec0070-d017-4d16-94f2-e82765e77583
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tadalafil
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA021368
Marketing category
NDA
Marketing start
2003-11-26
Marketing end
0000-00-00
Substance
TADALAFIL
Active strength
20 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

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-7145-16362971450130 TABLET, FILM COATED in 1 BOTTLE (63629-7145-1) 2016-11-290000-00-00NoNoCurrent
63629-7145-2636297145026 TABLET, FILM COATED in 1 BOTTLE (63629-7145-2) 2016-11-290000-00-00NoNoCurrent
63629-7145-36362971450310 TABLET, FILM COATED in 1 BOTTLE (63629-7145-3) 2016-11-290000-00-00NoNoCurrent
63629-7145-4636297145048 TABLET, FILM COATED in 1 BOTTLE (63629-7145-4) 2016-11-290000-00-00NoNoCurrent