NDC 0904-6671 – Sildenafil

Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0904-6671

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091479
Marketed since
November 6, 2012
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (2)

Package NDCDescriptionSince
0904-6671-0430 BLISTER PACK in 1 CARTON (0904-6671-04) / 1 TABLET, FILM COATED in 1 BLISTER PACKNov 6, 2012
0904-6671-0650 BLISTER PACK in 1 CARTON (0904-6671-06) / 1 TABLET, FILM COATED in 1 BLISTER PACKNov 6, 2012

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