telmisartan

Generic: telmisartan

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 20 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-087
Product ID 62332-087_eee590f3-5296-4091-a146-e4feedf76565
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202130
Listing Expiration 2026-12-31
Marketing Start 2016-06-25

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 62332087
Hyphenated Format 62332-087

Supplemental Identifiers

RxCUI
205304 205305 282755
UPC
0362332087303 0362332088300 0362332089307
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 ANDA202130 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 CARTON (62332-087-10)
  • 30 TABLET in 1 BOTTLE (62332-087-30)
  • 1000 TABLET in 1 BOTTLE (62332-087-91)
source: ndc

Packages (3)

62332-087-10 100 TABLET in 1 CARTON (62332-087-10) 62332-087-30 30 TABLET in 1 BOTTLE (62332-087-30) 62332-087-91 1000 TABLET in 1 BOTTLE (62332-087-91)

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": "eee590f3-5296-4091-a146-e4feedf76565", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0362332087303", "0362332088300", "0362332089307"], "unii": ["U5SYW473RQ"], "rxcui": ["205304", "205305", "282755"], "spl_set_id": ["c62d424c-7630-413c-be2c-3932831c3f1d"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (62332-087-10)", "package_ndc": "62332-087-10", "marketing_start_date": "20160625"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-087-30)", "package_ndc": "62332-087-30", "marketing_start_date": "20160625"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-087-91)", "package_ndc": "62332-087-91", "marketing_start_date": "20160625"}], "brand_name": "Telmisartan", "product_id": "62332-087_eee590f3-5296-4091-a146-e4feedf76565", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-087", "generic_name": "Telmisartan", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "20 mg/1"}], "application_number": "ANDA202130", "marketing_category": "ANDA", "marketing_start_date": "20160625", "listing_expiration_date": "20261231"}