telmisartan
Generic: telmisartan
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
telmisartan
Generic Name
telmisartan
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
telmisartan 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-4034
Product ID
68788-4034_bf8e95fa-d181-4b46-8609-497e14a73dc1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090032
Listing Expiration
2026-12-31
Marketing Start
2025-09-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687884034
Hyphenated Format
68788-4034
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68788-4034-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf8e95fa-d181-4b46-8609-497e14a73dc1", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205304"], "spl_set_id": ["bf8e95fa-d181-4b46-8609-497e14a73dc1"], "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 (68788-4034-3)", "package_ndc": "68788-4034-3", "marketing_start_date": "20250929"}], "brand_name": "Telmisartan", "product_id": "68788-4034_bf8e95fa-d181-4b46-8609-497e14a73dc1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-4034", "generic_name": "Telmisartan", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "40 mg/1"}], "application_number": "ANDA090032", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}