tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2217
Product ID
72162-2217_566e638b-1851-45e0-b04e-9c547be44c27
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202433
Listing Expiration
2026-12-31
Marketing Start
2013-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622217
Hyphenated Format
72162-2217
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
tamsulosin hydrochloride (source: ndc)
Generic Name
tamsulosin hydrochloride (source: ndc)
Application Number
ANDA202433 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/1
Packaging
- 500 CAPSULE in 1 BOTTLE (72162-2217-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "566e638b-1851-45e0-b04e-9c547be44c27", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["fd73ddfd-3773-45b2-9795-9e58744a6803"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72162-2217-5)", "package_ndc": "72162-2217-5", "marketing_start_date": "20240105"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "72162-2217_566e638b-1851-45e0-b04e-9c547be44c27", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72162-2217", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA202433", "marketing_category": "ANDA", "marketing_start_date": "20130430", "listing_expiration_date": "20261231"}