telmisartan

Generic: telmisartan

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 40 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-832
Product ID 72603-832_9c22a318-d1f2-4788-9331-66fed71ebf38
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203986
Listing Expiration 2026-12-31
Marketing Start 2025-12-01

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 72603832
Hyphenated Format 72603-832

Supplemental Identifiers

RxCUI
205304 205305 282755
UPC
0372603831016 0372603832013 0372603833010
UNII
U5SYW473RQ
NUI
N0000000070 N0000175561

Packaging Origin

Original Packager
true

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 ANDA203986 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 CONTAINER (72603-832-01)
source: ndc

Packages (1)

72603-832-01 30 TABLET in 1 CONTAINER (72603-832-01)

Ingredients (1)

telmisartan (40 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": "9c22a318-d1f2-4788-9331-66fed71ebf38", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0372603831016", "0372603832013", "0372603833010"], "unii": ["U5SYW473RQ"], "rxcui": ["205304", "205305", "282755"], "spl_set_id": ["9c22a318-d1f2-4788-9331-66fed71ebf38"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 CONTAINER (72603-832-01)", "package_ndc": "72603-832-01", "marketing_start_date": "20251201"}], "brand_name": "Telmisartan", "product_id": "72603-832_9c22a318-d1f2-4788-9331-66fed71ebf38", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72603-832", "generic_name": "Telmisartan", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "40 mg/1"}], "application_number": "ANDA203986", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}