NDC 68071-3892-01 - Telmisartan

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: 68071-3892
Requested NDC: 68071-3892-01
Package NDCs from labels: 68071-3892-1, 68071-3892-01
Manufacturer: NuCare Pharmaceuticals, Inc.
Effective date: 2025-09-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Telmisartan - NuCare Pharmaceuticals, Inc.	NuCare Pharmaceuticals, Inc.	2025-09-17	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68071-3892-1	Telmisartan	100 in 1 BOTTLE	TABLET	100		1

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 4 of 4 · 62 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
telmisartan	TELMISARTAN	Proficient Rx LP	593a53a4-91bc-4e4a-aeff-08fc2efe3dd4	2020-06-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205305 unii: U5SYW473RQ
Telmisartan and Amlodipine	TELMISARTAN AND AMLODIPINE	Mylan Pharmaceuticals Inc.	ca60a4d5-ace7-4889-94ee-e2265fd63811	2018-11-14	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: U5SYW473RQ

Reported adverse events (FAERS/openFDA)#

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