NDC 51655-033

Carvedilol 25 mg tablet, film coated

On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-165.

India: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action
Glenmark Pharmaceuticals LimitedDhar, IndiaMakes it and tests it Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Carvedilol: every company that makes it
Form
tablet, film coated, oral
Strength
25 mg
Approval
ANDA ANDA078251
On the market since
Sep 29, 2020
Package NDCs
51655-033-25 51655-033-26
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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