telmisartan
Generic: telmisartan
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
telmisartan
Generic Name
telmisartan
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
telmisartan 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5492
Product ID
50090-5492_6ec2fad4-f0a6-4039-980d-0075f5174d90
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202397
Listing Expiration
2026-12-31
Marketing Start
2014-07-07
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905492
Hyphenated Format
50090-5492
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
ANDA202397 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (50090-5492-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6ec2fad4-f0a6-4039-980d-0075f5174d90", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205305"], "spl_set_id": ["509cd338-24db-41d1-a115-9dc999170717"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (50090-5492-0)", "package_ndc": "50090-5492-0", "marketing_start_date": "20210316"}], "brand_name": "Telmisartan", "product_id": "50090-5492_6ec2fad4-f0a6-4039-980d-0075f5174d90", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-5492", "generic_name": "telmisartan", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA202397", "marketing_category": "ANDA", "marketing_start_date": "20140707", "listing_expiration_date": "20261231"}