NDC 71335-2191-01 - 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
- 71335-2191
- Requested NDC
- 71335-2191-01
- Package NDCs from labels
- 71335-2191-1, 71335-2191-2, 71335-2191-3, 71335-2191-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2026-05-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Telmisartan - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-05-22 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-2191-1 | Telmisartan | 90 in 1 BOTTLE | TABLET | 90 | 102 | |
| 71335-2191-2 | Telmisartan | 30 in 1 BOTTLE | TABLET | 30 | 102 | |
| 71335-2191-3 | Telmisartan | 180 in 1 BOTTLE | TABLET | 180 | 102 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-2191 | TELMISARTAN TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, Legacy NDC, 3 package rows | 20231121_830741dd-3f3c-4f8e-88c6-dc112166f477.zip |
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.
| 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 | 205305 U5SYW473RQ |
| Telmisartan and Amlodipine | TELMISARTAN AND AMLODIPINE | Mylan Pharmaceuticals Inc. | ca60a4d5-ace7-4889-94ee-e2265fd63811 | 2018-11-14 | Boxed warning, Warnings, Adverse reactions | U5SYW473RQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.