tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: amneal pharmaceuticals of new york llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler amneal pharmaceuticals of new york llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Amneal Pharmaceuticals of New York LLC

Identifiers & Regulatory

Product NDC 0115-8211
Product ID 0115-8211_e62d078e-2896-4acd-bcaa-c21e855e66e1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090377
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01158211
Hyphenated Format 0115-8211

Supplemental Identifiers

RxCUI
863669
UPC
0301158211011
UNII
11SV1951MR

Packaging Origin

Original Packager
true

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 ANDA090377 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0115-8211-01)
source: ndc

Packages (1)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e62d078e-2896-4acd-bcaa-c21e855e66e1", "openfda": {"upc": ["0301158211011"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["c3ae55dd-6a0e-4f3a-82b6-2448e0545550"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0115-8211-01)", "package_ndc": "0115-8211-01", "marketing_start_date": "20250401"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "0115-8211_e62d078e-2896-4acd-bcaa-c21e855e66e1", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0115-8211", "generic_name": "TAMSULOSIN HYDROCHLORIDE", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090377", "marketing_category": "ANDA", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}