terazosin
Generic: terazosin
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
terazosin
Generic Name
terazosin
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
terazosin hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-4064
Product ID
68788-4064_d1718217-ddab-4a3a-a862-8c952fd5a274
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075667
Listing Expiration
2027-12-31
Marketing Start
2026-01-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687884064
Hyphenated Format
68788-4064
Supplemental Identifiers
RxCUI
UNII
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
- 2 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (68788-4064-1)
- 30 CAPSULE in 1 BOTTLE (68788-4064-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d1718217-ddab-4a3a-a862-8c952fd5a274", "openfda": {"unii": ["D32S14F082"], "rxcui": ["313217"], "spl_set_id": ["d1718217-ddab-4a3a-a862-8c952fd5a274"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68788-4064-1)", "package_ndc": "68788-4064-1", "marketing_start_date": "20260128"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-4064-3)", "package_ndc": "68788-4064-3", "marketing_start_date": "20260128"}], "brand_name": "Terazosin", "product_id": "68788-4064_d1718217-ddab-4a3a-a862-8c952fd5a274", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68788-4064", "generic_name": "Terazosin", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075667", "marketing_category": "ANDA", "marketing_start_date": "20260128", "listing_expiration_date": "20271231"}