Sildenafil

Product NDC

68084-869

11-digit product format

680840869

Labeler code

68084

Product ID

68084-869_8346578a-72c6-6b02-e053-2991aa0af86b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA202025

Marketing category

ANDA

Marketing start

2015-02-25

Marketing end

2020-01-31

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

0000-00-00

Current FDA listing

Historical FDA.report record