tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler northstar rx llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-115
Product ID 72603-115_d26ad47b-f3ef-45d6-b39d-f64929a54489
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2026-12-31
Marketing Start 2013-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603115
Hyphenated Format 72603-115

Supplemental Identifiers

RxCUI
863669
UPC
0372603115017
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 ANDA202433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (72603-115-01)
  • 500 CAPSULE in 1 BOTTLE (72603-115-02)
source: ndc

Packages (2)

72603-115-01 100 CAPSULE in 1 BOTTLE (72603-115-01) 72603-115-02 500 CAPSULE in 1 BOTTLE (72603-115-02)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/1)

Linked Drug Pages (1)

Tamsulosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d26ad47b-f3ef-45d6-b39d-f64929a54489", "openfda": {"upc": ["0372603115017"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["7ab14f88-414a-448f-b7bf-de8c9e1b1eb3"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72603-115-01)", "package_ndc": "72603-115-01", "marketing_start_date": "20130430"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72603-115-02)", "package_ndc": "72603-115-02", "marketing_start_date": "20130430"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "72603-115_d26ad47b-f3ef-45d6-b39d-f64929a54489", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72603-115", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "NorthStar Rx LLC", "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"}