telmisartan

Generic: telmisartan

Labeler: cadila pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler cadila pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 80 mg/1

Manufacturer
Cadila Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 71209-051
Product ID 71209-051_a19404d0-fd12-42ab-b469-b8c7d1d5e7eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208605
Listing Expiration 2026-12-31
Marketing Start 2015-02-05

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 71209051
Hyphenated Format 71209-051

Supplemental Identifiers

RxCUI
205304 205305 282755
UPC
0371209051118 0371209049054 0371209051101 0371209050012 0371209049115 0371209050104 0371209049016 0371209049108 0371209050043 0371209051040 0371209050111
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 ANDA208605 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71209-051-01)
  • 90 TABLET in 1 BOTTLE (71209-051-04)
  • 100 TABLET in 1 BOTTLE (71209-051-05)
  • 500 TABLET in 1 BOTTLE (71209-051-10)
  • 1000 TABLET in 1 BOTTLE (71209-051-11)
  • 30 BLISTER PACK in 1 CARTON (71209-051-16) / 10 TABLET in 1 BLISTER PACK
  • 30 BLISTER PACK in 1 CARTON (71209-051-18) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (7)

Ingredients (1)

telmisartan (80 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a19404d0-fd12-42ab-b469-b8c7d1d5e7eb", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0371209051118", "0371209049054", "0371209051101", "0371209050012", "0371209049115", "0371209050104", "0371209049016", "0371209049108", "0371209050043", "0371209051040", "0371209050111"], "unii": ["U5SYW473RQ"], "rxcui": ["205304", "205305", "282755"], "spl_set_id": ["353fcb30-2fa7-4ff1-8a18-26f3ec279d00"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71209-051-01)", "package_ndc": "71209-051-01", "marketing_start_date": "20221222"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71209-051-04)", "package_ndc": "71209-051-04", "marketing_start_date": "20221222"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-051-05)", "package_ndc": "71209-051-05", "marketing_start_date": "20221222"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71209-051-10)", "package_ndc": "71209-051-10", "marketing_start_date": "20221222"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71209-051-11)", "package_ndc": "71209-051-11", "marketing_start_date": "20221222"}, {"sample": false, "description": "30 BLISTER PACK in 1 CARTON (71209-051-16)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "71209-051-16", "marketing_start_date": "20150205"}, {"sample": false, "description": "30 BLISTER PACK in 1 CARTON (71209-051-18)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "71209-051-18", "marketing_start_date": "20150205"}], "brand_name": "Telmisartan", "product_id": "71209-051_a19404d0-fd12-42ab-b469-b8c7d1d5e7eb", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71209-051", "generic_name": "Telmisartan", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "80 mg/1"}], "application_number": "ANDA208605", "marketing_category": "ANDA", "marketing_start_date": "20150205", "listing_expiration_date": "20261231"}