micardis

Generic: telmisartan

Labeler: boehringer ingelheim pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name micardis
Generic Name telmisartan
Labeler boehringer ingelheim pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 40 mg/1

Manufacturer
Boehringer Ingelheim Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0597-0040
Product ID 0597-0040_333f0ca9-928d-45af-92b9-9ea8a4d02f7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020850
Marketing Start 2000-12-01
Marketing End 2026-06-30

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 05970040
Hyphenated Format 0597-0040

Supplemental Identifiers

RxCUI
205304 205305 213431 213432 282755 284531
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 micardis (source: ndc)
Generic Name telmisartan (source: ndc)
Application Number NDA020850 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (0597-0040-37) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

telmisartan (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "333f0ca9-928d-45af-92b9-9ea8a4d02f7d", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["U5SYW473RQ"], "rxcui": ["205304", "205305", "213431", "213432", "282755", "284531"], "spl_set_id": ["cfb9309f-e0df-4a55-9542-0e869fce05fb"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Boehringer Ingelheim Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0597-0040-37)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "0597-0040-37", "marketing_end_date": "20260630", "marketing_start_date": "20001201"}], "brand_name": "Micardis", "product_id": "0597-0040_333f0ca9-928d-45af-92b9-9ea8a4d02f7d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "0597-0040", "generic_name": "telmisartan", "labeler_name": "Boehringer Ingelheim Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Micardis", "active_ingredients": [{"name": "TELMISARTAN", "strength": "40 mg/1"}], "application_number": "NDA020850", "marketing_category": "NDA", "marketing_end_date": "20260630", "marketing_start_date": "20001201"}