telmisartan

Generic: telmisartan

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 80 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1723
Product ID 71335-1723_3a6a5bb0-26f7-43df-a8ff-c5ac63798b97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090032
Listing Expiration 2026-12-31
Marketing Start 2014-07-07

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351723
Hyphenated Format 71335-1723

Supplemental Identifiers

RxCUI
205305
UNII
U5SYW473RQ
NUI
N0000000070 N0000175561

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name telmisartan (source: ndc)
Generic Name telmisartan (source: ndc)
Application Number ANDA090032 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-1723-1)
  • 30 TABLET in 1 BOTTLE (71335-1723-2)
source: ndc

Packages (2)

Ingredients (1)

telmisartan (80 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a6a5bb0-26f7-43df-a8ff-c5ac63798b97", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205305"], "spl_set_id": ["c55e4fe1-f04d-4995-a706-9f432fde57e4"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1723-1)", "package_ndc": "71335-1723-1", "marketing_start_date": "20240404"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1723-2)", "package_ndc": "71335-1723-2", "marketing_start_date": "20201020"}], "brand_name": "Telmisartan", "product_id": "71335-1723_3a6a5bb0-26f7-43df-a8ff-c5ac63798b97", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-1723", "generic_name": "Telmisartan", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA090032", "marketing_category": "ANDA", "marketing_start_date": "20140707", "listing_expiration_date": "20261231"}