Sildenafil

Product NDC

50090-2858

11-digit product format

500902858

Labeler code

50090

Product ID

50090-2858_fa45d49d-6d88-48b2-8d70-a5195cb294a4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA203963

Marketing category

ANDA

Marketing start

2015-11-18

Marketing end

0000-00-00

Substance

SILDENAFIL CITRATE

Active strength

20 mg/1

Pharmacologic classes

Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record