Sildenafil

Product NDC

70934-208

11-digit product format

709340208

Labeler code

70934

Product ID

70934-208_86bfc059-5307-206a-e053-2a91aa0ac37c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Denton Pharma, Inc. DBA Northwind Pharmaceuticals

Application

ANDA078380

Marketing category

ANDA

Marketing start

2018-12-17

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

2020-12-31

Current FDA listing

Historical FDA.report record