NDC 60290-030 – Tadalafil

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

Human Prescription Drug

Product NDC60290-030

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Umedica Laboratories USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211298
Marketed since
February 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (5)

Package NDCDescriptionSince
60290-030-0130 TABLET, FILM COATED in 1 BOTTLE (60290-030-01)Feb 15, 2026
60290-030-021000 TABLET, FILM COATED in 1 BOTTLE (60290-030-02)Feb 15, 2026
60290-030-0330 TABLET, FILM COATED in 1 BLISTER PACK (60290-030-03)Feb 15, 2026
60290-030-04500 TABLET, FILM COATED in 1 BOTTLE (60290-030-04)Apr 24, 2026
60290-030-055000 TABLET, FILM COATED in 1 BOTTLE (60290-030-05)Apr 24, 2026

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