trandolapril

Generic: trandolapril

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trandolapril
Generic Name trandolapril
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

trandolapril 2 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1431
Product ID 71335-1431_43db4bac-8048-4f48-8325-4915515f31a4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078438
Listing Expiration 2026-12-31
Marketing Start 2007-06-12

Pharmacologic Class

Established (EPC)
angiotensin converting enzyme inhibitor [epc]
Mechanism of Action
angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351431
Hyphenated Format 71335-1431

Supplemental Identifiers

RxCUI
199351
UNII
1T0N3G9CRC
NUI
N0000175562 N0000000181

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 trandolapril (source: ndc)
Generic Name trandolapril (source: ndc)
Application Number ANDA078438 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1431-1)
  • 90 TABLET in 1 BOTTLE (71335-1431-2)
source: ndc

Packages (2)

Ingredients (1)

trandolapril (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43db4bac-8048-4f48-8325-4915515f31a4", "openfda": {"nui": ["N0000175562", "N0000000181"], "unii": ["1T0N3G9CRC"], "rxcui": ["199351"], "spl_set_id": ["57f8aac6-3bd3-4ae1-aab2-759c8bc23292"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1431-1)", "package_ndc": "71335-1431-1", "marketing_start_date": "20191206"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1431-2)", "package_ndc": "71335-1431-2", "marketing_start_date": "20240530"}], "brand_name": "Trandolapril", "product_id": "71335-1431_43db4bac-8048-4f48-8325-4915515f31a4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-1431", "generic_name": "Trandolapril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trandolapril", "active_ingredients": [{"name": "TRANDOLAPRIL", "strength": "2 mg/1"}], "application_number": "ANDA078438", "marketing_category": "ANDA", "marketing_start_date": "20070612", "listing_expiration_date": "20261231"}