NDC 71821-007 – Tadalafil

Tadalafil 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71821-007

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
VKT Pharma Private Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215556
Marketed since
November 4, 2021
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (2)

Package NDCDescriptionSince
71821-007-0115 CARTON in 1 BLISTER PACK (71821-007-01) / 30 TABLET, FILM COATED in 1 CARTONNov 4, 2021
71821-007-0230 TABLET, FILM COATED in 1 BOTTLE (71821-007-02)Nov 4, 2021

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