terazosin

Generic: terazosin hydrochloride

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

Drug Facts

Product Profile

Brand Name terazosin
Generic Name terazosin hydrochloride
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

terazosin hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1702
Product ID 72162-1702_a55a5e8b-d486-40ea-9d43-d296e6fc2a9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075317
Listing Expiration 2026-12-31
Marketing Start 2004-12-20

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621702
Hyphenated Format 72162-1702

Supplemental Identifiers

RxCUI
260376
UNII
D32S14F082

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 terazosin (source: ndc)
Generic Name terazosin hydrochloride (source: ndc)
Application Number ANDA075317 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1000 CAPSULE in 1 BOTTLE (72162-1702-0)
  • 100 CAPSULE in 1 BOTTLE (72162-1702-1)
source: ndc

Packages (2)

Ingredients (1)

terazosin hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a55a5e8b-d486-40ea-9d43-d296e6fc2a9f", "openfda": {"unii": ["D32S14F082"], "rxcui": ["260376"], "spl_set_id": ["458b4a60-b2d6-445a-8638-7fcd07decf66"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72162-1702-0)", "package_ndc": "72162-1702-0", "marketing_start_date": "20231207"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72162-1702-1)", "package_ndc": "72162-1702-1", "marketing_start_date": "20231207"}], "brand_name": "Terazosin", "product_id": "72162-1702_a55a5e8b-d486-40ea-9d43-d296e6fc2a9f", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1702", "generic_name": "Terazosin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075317", "marketing_category": "ANDA", "marketing_start_date": "20041220", "listing_expiration_date": "20261231"}