Sildenafil

Product NDC

70518-0438

11-digit product format

705180438

Labeler code

70518

Product ID

70518-0438_85015dfa-a965-5937-e053-2991aa0a37d6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA203814

Marketing category

ANDA

Marketing start

2017-04-19

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