tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: synthon pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler synthon pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Synthon Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 63672-0021
Product ID 63672-0021_44e3098a-c374-d7aa-e063-6294a90aef5d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078801
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 636720021
Hyphenated Format 63672-0021

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 ANDA078801 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 20000 CAPSULE in 1 DRUM (63672-0021-9)
source: ndc

Packages (1)

63672-0021-9 20000 CAPSULE in 1 DRUM (63672-0021-9)

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": "44e3098a-c374-d7aa-e063-6294a90aef5d", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["13a5032d-0be1-4001-916e-459f0b1a051d"], "manufacturer_name": ["Synthon Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20000 CAPSULE in 1 DRUM (63672-0021-9)", "package_ndc": "63672-0021-9", "marketing_start_date": "20240115"}], "brand_name": "Tamsulosin hydrochloride", "product_id": "63672-0021_44e3098a-c374-d7aa-e063-6294a90aef5d", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "63672-0021", "generic_name": "tamsulosin hydrochloride", "labeler_name": "Synthon Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA078801", "marketing_category": "ANDA", "marketing_start_date": "20100427", "listing_expiration_date": "20261231"}