telmisartan

Generic: telmisartan

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name telmisartan
Generic Name telmisartan
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

telmisartan 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-371
Product ID 72789-371_34184fdf-e74f-fa7f-e063-6294a90a66c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205150
Listing Expiration 2026-12-31
Marketing Start 2016-06-12

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 72789371
Hyphenated Format 72789-371

Supplemental Identifiers

RxCUI
282755
UPC
0372789371900
UNII
U5SYW473RQ
NUI
N0000000070 N0000175561

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 ANDA205150 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-371-90)
source: ndc

Packages (1)

72789-371-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-371-90)

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": "34184fdf-e74f-fa7f-e063-6294a90a66c3", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0372789371900"], "unii": ["U5SYW473RQ"], "rxcui": ["282755"], "spl_set_id": ["56a72ddf-c2a2-45ce-91b1-1fcfbff52c10"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-371-90)", "package_ndc": "72789-371-90", "marketing_start_date": "20240123"}], "brand_name": "telmisartan", "product_id": "72789-371_34184fdf-e74f-fa7f-e063-6294a90a66c3", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-371", "generic_name": "telmisartan", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "telmisartan", "active_ingredients": [{"name": "TELMISARTAN", "strength": "20 mg/1"}], "application_number": "ANDA205150", "marketing_category": "ANDA", "marketing_start_date": "20160612", "listing_expiration_date": "20261231"}