telmisartan

Generic: telmisartan

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 20 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8441
Product ID 68788-8441_25a84cb9-ebc2-402e-80d1-9170b6500174
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205150
Listing Expiration 2026-12-31
Marketing Start 2023-05-02

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 687888441
Hyphenated Format 68788-8441

Supplemental Identifiers

RxCUI
282755
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 ANDA205150 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-8441-3)
  • 60 TABLET in 1 BOTTLE (68788-8441-6)
  • 90 TABLET in 1 BOTTLE (68788-8441-9)
source: ndc

Packages (3)

68788-8441-3 30 TABLET in 1 BOTTLE (68788-8441-3) 68788-8441-6 60 TABLET in 1 BOTTLE (68788-8441-6) 68788-8441-9 90 TABLET in 1 BOTTLE (68788-8441-9)

Ingredients (1)

telmisartan (20 mg/1)

Linked Drug Pages (1)

telmisartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "25a84cb9-ebc2-402e-80d1-9170b6500174", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["282755"], "spl_set_id": ["f6da5155-9c26-46bb-bc0f-ece4ea21405f"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8441-3)", "package_ndc": "68788-8441-3", "marketing_start_date": "20230502"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8441-6)", "package_ndc": "68788-8441-6", "marketing_start_date": "20230502"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8441-9)", "package_ndc": "68788-8441-9", "marketing_start_date": "20230502"}], "brand_name": "telmisartan", "product_id": "68788-8441_25a84cb9-ebc2-402e-80d1-9170b6500174", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-8441", "generic_name": "telmisartan", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "20 mg/1"}], "application_number": "ANDA205150", "marketing_category": "ANDA", "marketing_start_date": "20230502", "listing_expiration_date": "20261231"}