terazosin
Generic: terazosin
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
terazosin
Generic Name
terazosin
Labeler
bionpharma inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
terazosin hydrochloride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-330
Product ID
69452-330_29b9921b-6884-e5bb-e063-6394a90aecf6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075667
Listing Expiration
2026-12-31
Marketing Start
2024-03-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452330
Hyphenated Format
69452-330
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Application Number
ANDA075667 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (69452-330-20)
- 1000 CAPSULE in 1 BOTTLE (69452-330-32)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29b9921b-6884-e5bb-e063-6394a90aecf6", "openfda": {"upc": ["0369452331323", "0369452330326", "0369452333327", "0369452332320"], "unii": ["D32S14F082"], "rxcui": ["260376", "313215", "313217", "313219"], "spl_set_id": ["130c84dc-b598-660f-e063-6294a90a8e46"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69452-330-20)", "package_ndc": "69452-330-20", "marketing_start_date": "20240311"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (69452-330-32)", "package_ndc": "69452-330-32", "marketing_start_date": "20241220"}], "brand_name": "Terazosin", "product_id": "69452-330_29b9921b-6884-e5bb-e063-6394a90aecf6", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "69452-330", "generic_name": "Terazosin", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA075667", "marketing_category": "ANDA", "marketing_start_date": "20240311", "listing_expiration_date": "20261231"}