NDC 68071-3777 – Tadalafil

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

Human Prescription Drug

Product NDC68071-3777

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209250
Marketed since
March 26, 2019
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (4)

Package NDCDescriptionSince
68071-3777-424 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-4)Jan 20, 2025
68071-3777-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-5)Jan 20, 2025
68071-3777-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-6)Apr 21, 2025
68071-3777-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3777-9)Jul 24, 2026

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