Sildenafil

Product NDC

55700-398

11-digit product format

557000398

Labeler code

55700

Product ID

55700-398_962d19fc-c704-49a4-8bb8-437abb6fdbca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality C

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