tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-598
Product ID 65862-598_94771a21-3051-46cc-8deb-200bc9f3dcb3
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 65862598
Hyphenated Format 65862-598

Supplemental Identifiers

RxCUI
863669
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 (65862-598-01)
  • 500 CAPSULE in 1 BOTTLE (65862-598-05)
  • 3 BLISTER PACK in 1 CARTON (65862-598-10) / 10 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (3)

65862-598-01 100 CAPSULE in 1 BOTTLE (65862-598-01) 65862-598-05 500 CAPSULE in 1 BOTTLE (65862-598-05) 65862-598-10 3 BLISTER PACK in 1 CARTON (65862-598-10) / 10 CAPSULE in 1 BLISTER PACK

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": "94771a21-3051-46cc-8deb-200bc9f3dcb3", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["8cb27f78-2d5d-4640-b7b5-ed06973c8133"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65862-598-01)", "package_ndc": "65862-598-01", "marketing_start_date": "20130430"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (65862-598-05)", "package_ndc": "65862-598-05", "marketing_start_date": "20130430"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (65862-598-10)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "65862-598-10", "marketing_start_date": "20130430"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "65862-598_94771a21-3051-46cc-8deb-200bc9f3dcb3", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "65862-598", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "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"}