NDC 60290-079 – Sildenafil Citrate

Sildenafil Citrate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60290-079

Product details

Brand name
Sildenafil Citrate
Generic name
Sildenafil Citrate
Labeler
Umedica Laboratories USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209302
Marketed since
February 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil Citrate →

Package NDC codes (4)

Package NDCDescriptionSince
60290-079-0130 TABLET, FILM COATED in 1 BOTTLE (60290-079-01)Feb 15, 2026
60290-079-0290 TABLET, FILM COATED in 1 BOTTLE (60290-079-02)Feb 15, 2026
60290-079-031000 TABLET, FILM COATED in 1 BOTTLE (60290-079-03)Feb 15, 2026
60290-079-04500 TABLET, FILM COATED in 1 BOTTLE (60290-079-04)Apr 27, 2026

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