telmisartan

Generic: telmisartan

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 20 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-312
Product ID 70756-312_28abd7a9-b660-4c91-b5f4-b65aa673fdbc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218157
Listing Expiration 2026-12-31
Marketing Start 2024-10-15

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 70756312
Hyphenated Format 70756-312

Supplemental Identifiers

RxCUI
205304 205305 282755
UPC
0370756313304 0370756314301
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 ANDA218157 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (70756-312-30)
  • 10 BLISTER PACK in 1 CARTON (70756-312-99) / 10 TABLET in 1 BLISTER PACK (70756-312-01)
source: ndc

Packages (2)

70756-312-30 30 TABLET in 1 BOTTLE (70756-312-30) 70756-312-99 10 BLISTER PACK in 1 CARTON (70756-312-99) / 10 TABLET in 1 BLISTER PACK (70756-312-01)

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": "28abd7a9-b660-4c91-b5f4-b65aa673fdbc", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0370756313304", "0370756314301"], "unii": ["U5SYW473RQ"], "rxcui": ["205304", "205305", "282755"], "spl_set_id": ["3ff464e6-7a36-4544-a06f-7848414f77fc"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-312-30)", "package_ndc": "70756-312-30", "marketing_start_date": "20241015"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70756-312-99)  / 10 TABLET in 1 BLISTER PACK (70756-312-01)", "package_ndc": "70756-312-99", "marketing_start_date": "20241015"}], "brand_name": "Telmisartan", "product_id": "70756-312_28abd7a9-b660-4c91-b5f4-b65aa673fdbc", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70756-312", "generic_name": "Telmisartan", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "20 mg/1"}], "application_number": "ANDA218157", "marketing_category": "ANDA", "marketing_start_date": "20241015", "listing_expiration_date": "20261231"}