tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3646
Product ID
50090-3646_0e5535f7-b97c-4e7a-96c5-58105c1c4519
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207405
Listing Expiration
2026-12-31
Marketing Start
2017-08-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500903646
Hyphenated Format
50090-3646
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
ANDA207405 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (50090-3646-0)
- 90 CAPSULE in 1 BOTTLE, PLASTIC (50090-3646-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e5535f7-b97c-4e7a-96c5-58105c1c4519", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["3a05970e-6c34-4dff-9fd7-dde8ce60f280"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-3646-0)", "package_ndc": "50090-3646-0", "marketing_start_date": "20181010"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (50090-3646-1)", "package_ndc": "50090-3646-1", "marketing_start_date": "20170811"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "50090-3646_0e5535f7-b97c-4e7a-96c5-58105c1c4519", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50090-3646", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA207405", "marketing_category": "ANDA", "marketing_start_date": "20170811", "listing_expiration_date": "20261231"}