Sildenafil

Product NDC

68071-1979

11-digit product format

680711979

Labeler code

68071

Product ID

68071-1979_4fbc055d-ea8e-5ac0-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Sildenafil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

2020-12-31

Current FDA listing

Historical FDA.report record