terazosin
Generic: terazosin hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
terazosin
Generic Name
terazosin hydrochloride
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
terazosin hydrochloride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0657
Product ID
50090-0657_d0073283-4e97-4e24-a94c-0240ff908c55
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075317
Listing Expiration
2026-12-31
Marketing Start
2004-12-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900657
Hyphenated Format
50090-0657
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 hydrochloride (source: ndc)
Application Number
ANDA075317 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (50090-0657-0)
- 90 CAPSULE in 1 BOTTLE (50090-0657-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d0073283-4e97-4e24-a94c-0240ff908c55", "openfda": {"unii": ["D32S14F082"], "rxcui": ["313215"], "spl_set_id": ["4b195327-10d4-477f-ada2-d62c7f835e6c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-0657-0)", "package_ndc": "50090-0657-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-0657-1)", "package_ndc": "50090-0657-1", "marketing_start_date": "20141128"}], "brand_name": "Terazosin", "product_id": "50090-0657_d0073283-4e97-4e24-a94c-0240ff908c55", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50090-0657", "generic_name": "Terazosin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terazosin", "active_ingredients": [{"name": "TERAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA075317", "marketing_category": "ANDA", "marketing_start_date": "20041220", "listing_expiration_date": "20261231"}