NDC 71205-736 – Tadalafil

Tadalafil 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-736

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209654
Marketed since
March 26, 2019
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (7)

Package NDCDescriptionSince
71205-736-1010 TABLET in 1 BOTTLE (71205-736-10)Mar 3, 2023
71205-736-1414 TABLET in 1 BOTTLE (71205-736-14)Mar 3, 2023
71205-736-1515 TABLET in 1 BOTTLE (71205-736-15)Mar 3, 2023
71205-736-2020 TABLET in 1 BOTTLE (71205-736-20)Mar 3, 2023
71205-736-3030 TABLET in 1 BOTTLE (71205-736-30)Dec 23, 2022
71205-736-6060 TABLET in 1 BOTTLE (71205-736-60)Dec 23, 2022
71205-736-9090 TABLET in 1 BOTTLE (71205-736-90)Dec 23, 2022

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