tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler macleods pharmaceuticals limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-159
Product ID 33342-159_95b0ff14-97b3-4b8c-8545-f066a45c2f82
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204645
Listing Expiration 2026-12-31
Marketing Start 2017-01-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342159
Hyphenated Format 33342-159

Supplemental Identifiers

RxCUI
863669
UPC
0333342159106 0333342159113
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 ANDA204645 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (33342-159-07)
  • 100 CAPSULE in 1 BOTTLE (33342-159-11)
  • 10 BLISTER PACK in 1 CARTON (33342-159-12) / 10 CAPSULE in 1 BLISTER PACK
  • 500 CAPSULE in 1 BOTTLE (33342-159-15)
  • 1000 CAPSULE in 1 BOTTLE (33342-159-44)
source: ndc

Packages (5)

33342-159-07 30 CAPSULE in 1 BOTTLE (33342-159-07) 33342-159-11 100 CAPSULE in 1 BOTTLE (33342-159-11) 33342-159-12 10 BLISTER PACK in 1 CARTON (33342-159-12) / 10 CAPSULE in 1 BLISTER PACK 33342-159-15 500 CAPSULE in 1 BOTTLE (33342-159-15) 33342-159-44 1000 CAPSULE in 1 BOTTLE (33342-159-44)

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": "95b0ff14-97b3-4b8c-8545-f066a45c2f82", "openfda": {"upc": ["0333342159106", "0333342159113"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["2912fbbc-89bf-4bf0-86fe-bd98f3168e84"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (33342-159-07)", "package_ndc": "33342-159-07", "marketing_start_date": "20170125"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (33342-159-11)", "package_ndc": "33342-159-11", "marketing_start_date": "20170125"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-159-12)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "33342-159-12", "marketing_start_date": "20170125"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (33342-159-15)", "package_ndc": "33342-159-15", "marketing_start_date": "20170125"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (33342-159-44)", "package_ndc": "33342-159-44", "marketing_start_date": "20170125"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "33342-159_95b0ff14-97b3-4b8c-8545-f066a45c2f82", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "33342-159", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA204645", "marketing_category": "ANDA", "marketing_start_date": "20170125", "listing_expiration_date": "20261231"}