FDA.reportPublic FDA data

VOSTALLY

Manufacturer
L M Manufacturing Limited
Effective date
2026-01-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:11

Label at a glance#

ProductVOSTALLY
Active ingredientRAMIPRIL
Label structure3 sections

Dosage and administration

Initial dose is 2.5 mg to 20 mg orally once daily.

Label contents#

Full prescribing information#

Indication and Usage

INDICATIONS & USAGE SECTION

The risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions

Dosage and Administration Section

DOSAGE & ADMINISTRATION SECTION

Initial dose is 2.5 mg to 20 mg orally once daily.

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VostallyVostally

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82565-00382565-003-15

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
RAMIPRILL35JN3I7SJACTIB

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
47de9205-fa5f-ff64-e063-6294a90ae71047de9205-fa5e-ff64-e063-6294a90ae7102026-01-08Exact identifier
spl id: 47de9205-fa5f-ff64-e063-6294a90ae710
spl set id: 47de9205-fa5e-ff64-e063-6294a90ae710

Reported adverse events (FAERS/openFDA)#

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