tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler sandoz inc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-2076
Product ID 0781-2076_98c2abd9-1998-48cd-83f9-f5f94ff39345
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078015
Listing Expiration 2026-12-31
Marketing Start 2010-04-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07812076
Hyphenated Format 0781-2076

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 ANDA078015 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0781-2076-01)
  • 1000 CAPSULE in 1 BOTTLE (0781-2076-10)
  • 90 CAPSULE in 1 BOTTLE (0781-2076-92)
source: ndc

Packages (3)

0781-2076-01 100 CAPSULE in 1 BOTTLE (0781-2076-01) 0781-2076-10 1000 CAPSULE in 1 BOTTLE (0781-2076-10) 0781-2076-92 90 CAPSULE in 1 BOTTLE (0781-2076-92)

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": "98c2abd9-1998-48cd-83f9-f5f94ff39345", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["fb120098-b007-4a33-80b8-b7279c7668ee"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0781-2076-01)", "package_ndc": "0781-2076-01", "marketing_start_date": "20100427"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (0781-2076-10)", "package_ndc": "0781-2076-10", "marketing_start_date": "20100427"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (0781-2076-92)", "package_ndc": "0781-2076-92", "marketing_start_date": "20190131"}], "brand_name": "tamsulosin hydrochloride", "product_id": "0781-2076_98c2abd9-1998-48cd-83f9-f5f94ff39345", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0781-2076", "generic_name": "tamsulosin hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tamsulosin hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078015", "marketing_category": "ANDA", "marketing_start_date": "20100427", "listing_expiration_date": "20261231"}