NDC 68788-8664 – Tadalafil

Tadalafil 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8664

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210609
Marketed since
May 13, 2024
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (3)

Package NDCDescriptionSince
68788-8664-115 TABLET in 1 BOTTLE (68788-8664-1)May 13, 2024
68788-8664-330 TABLET in 1 BOTTLE (68788-8664-3)May 13, 2024
68788-8664-77 TABLET in 1 BOTTLE (68788-8664-7)May 13, 2024

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