NDC 70771-1977 - ZYCUBO

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 70771-1977
Package NDCs from labels: 70771-1977-1
Manufacturer: Zydus Lifesciences Limited
Effective date: 2026-01-27
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ZYCUBO - Zydus Lifesciences Limited	Zydus Lifesciences Limited	2026-01-27	HUMAN PRESCRIPTION DRUG LABEL

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
de97d0e2-2076-47d1-b87e-1a903fda4778			a1c4fdde-0ffb-4742-b042-b0e29460cf13	2026-01-27		Exact identifier spl id: de97d0e2-2076-47d1-b87e-1a903fda4778 spl set id: a1c4fdde-0ffb-4742-b042-b0e29460cf13
Zycubo	COPPER HISTIDINATE	Sentynl Therapeutics, Inc.	e3aeefc2-f44d-4337-9c2e-3dba44a89e48	2026-01-12	Warnings, Adverse reactions	Exact identifier unii: 9078K3MO9U

Reported adverse events (FAERS/openFDA)#

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