tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

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

Drug Facts

Product Profile

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

tamsulosin hydrochloride .4 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 72865-282
Product ID 72865-282_cef0532b-bdf6-44e8-85a7-f302aa853949
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214730
Listing Expiration 2026-12-31
Marketing Start 2024-09-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865282
Hyphenated Format 72865-282

Supplemental Identifiers

RxCUI
863669
UPC
0372865282052 0372865282908 0372865282014
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 ANDA214730 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (72865-282-01)
  • 500 CAPSULE in 1 BOTTLE (72865-282-05)
  • 90 CAPSULE in 1 BOTTLE (72865-282-90)
source: ndc

Packages (3)

72865-282-01 100 CAPSULE in 1 BOTTLE (72865-282-01) 72865-282-05 500 CAPSULE in 1 BOTTLE (72865-282-05) 72865-282-90 90 CAPSULE in 1 BOTTLE (72865-282-90)

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": "cef0532b-bdf6-44e8-85a7-f302aa853949", "openfda": {"upc": ["0372865282052", "0372865282908", "0372865282014"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["9108b999-4b99-469d-99a8-5ef0fa4ca00a"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72865-282-01)", "package_ndc": "72865-282-01", "marketing_start_date": "20240910"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72865-282-05)", "package_ndc": "72865-282-05", "marketing_start_date": "20250226"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72865-282-90)", "package_ndc": "72865-282-90", "marketing_start_date": "20250226"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "72865-282_cef0532b-bdf6-44e8-85a7-f302aa853949", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72865-282", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA214730", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20261231"}