NDC 76420-857 – Tadalafil

Tadalafil 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC76420-857

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209250
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 (5)

Package NDCDescriptionSince
76420-857-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-857-01)Jan 28, 2025
76420-857-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-857-05)Jan 28, 2025
76420-857-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-857-30)Jan 28, 2025
76420-857-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-857-60)Jan 28, 2025
76420-857-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-857-90)Jan 28, 2025

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