FDA.reportPublic FDA data

Vybrique

Manufacturer
Altergon Italia SRL
Effective date
2026-01-26
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:05

Label at a glance#

ProductVybrique
Active ingredientSILDENAFIL CITRATE
Label structure13 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Vybrique is indicated for erectile dysfunction

Vybrique 25 mg 2 pack sample

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-016-02

Vybrique 25mg

sildenafil oral film

2 pack sample

25 mg 2 pack25 mg 2 pack

Vibrique 25 mg 4 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vybrique

Sildeanfil Oral Film

4 pack

25 mg 4 pack25 mg 4 pack

Vybrique 25 mg 8 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-016-08

Vybrique 25 mg

sildenafil oral film

8 pack

25 mg 8 pack25 mg 8 pack

Vybrique 50 mg 2 pack sample

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-017-02

Vybrique 50 mg

sildenafil oral film

2 pack sample

50 mg 2 pack50 mg 2 pack

Vybrique 50 mg 4 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-017-04

Vybrique 50 mg

sildenafil oral film

4 pack

50 mg 4 pack50 mg 4 pack

Vybrique 50 mg 8 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-017-08

Vybrique 50 mg

sildenafil oral film

8 pack

50 mg 8 pack50 mg 8 pack

Vybrique 75 mg 2 pack sample

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-018-02

Vybrique 75 mg

sildenafil oral film

2 pack sample

75 mg 2 pack75 mg 2 pack

Vybrique 75 mg 4 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-018-04

Vybrique 75 mg

sildenafil oral film

4 pack

75 mg 4 pack75 mg 4 pack

Vybrique 75 mg 8 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-018-08

Vybrique 75 mg

sildenafil oral film

8 pack

75 mg 8 pack75 mg 8 pack

Vybrique 100 mg 2 pack sample

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-019-02

Vybrique 100 mg

sildenafil oral film

2 pack sample

100 mg 2pack100 mg 2pack

Vybrique 100 mg 4 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-019-04

Vybrique 100 mg

sildenafil oral film

4 pack

100 mg 4 pack100 mg 4 pack

Vybrique 100 mg 8 pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 43328-019-08

Vybrique 100 mg

sildenafil oral film

8 pack

100 mg 8 pack100 mg 8 pack

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43328-01643328-016-01, 43328-016-04, 43328-016-08, 43328-016-02
43328-01943328-019-01, 43328-019-04, 43328-019-08, 43328-019-02
43328-01843328-018-01, 43328-018-04, 43328-018-08, 43328-018-02
43328-01743328-017-01, 43328-017-04, 43328-017-08, 43328-017-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
SUCRALOSE96K6UQ3ZD4IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FD&C BLUE NO. 2L06K8R7DQKIACT
PROPYLENE GLYCOL MONOCAPRYLATERT9P9S09QIIACT
SILDENAFIL CITRATEBW9B0ZE037ACTIM
MALTODEXTRIN7CVR7L4A2DIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
MALTODEXTRIN7CVR7L4A2DIACT
SUCRALOSE96K6UQ3ZD4IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FD&C BLUE NO. 2L06K8R7DQKIACT
PROPYLENE GLYCOL MONOCAPRYLATERT9P9S09QIIACT
SILDENAFIL CITRATEBW9B0ZE037ACTIM
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
MALTODEXTRIN7CVR7L4A2DIACT
SUCRALOSE96K6UQ3ZD4IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FD&C BLUE NO. 2L06K8R7DQKIACT
PROPYLENE GLYCOL MONOCAPRYLATERT9P9S09QIIACT
SILDENAFIL CITRATEBW9B0ZE037ACTIM
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
MALTODEXTRIN7CVR7L4A2DIACT
SUCRALOSE96K6UQ3ZD4IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FD&C BLUE NO. 2L06K8R7DQKIACT
PROPYLENE GLYCOL MONOCAPRYLATERT9P9S09QIIACT
SILDENAFIL CITRATEBW9B0ZE037ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4833eb62-25f7-d68d-e063-6294a90ab8174833eb62-25f6-d68d-e063-6294a90ab8172026-01-26Exact identifier
spl id: 4833eb62-25f7-d68d-e063-6294a90ab817
spl set id: 4833eb62-25f6-d68d-e063-6294a90ab817

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.