tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

tamsulosin hydrochloride .4 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-740
Product ID 50268-740_41c4deb3-2dcf-b17a-e063-6294a90ad2be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207405
Listing Expiration 2026-12-31
Marketing Start 2018-01-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268740
Hyphenated Format 50268-740

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 ANDA207405 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX (50268-740-01) / 1 CAPSULE in 1 BLISTER PACK (50268-740-11)
  • 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-740-15) / 1 CAPSULE in 1 BLISTER PACK (50268-740-11)
source: ndc

Packages (2)

50268-740-01 100 BLISTER PACK in 1 BOX (50268-740-01) / 1 CAPSULE in 1 BLISTER PACK (50268-740-11) 50268-740-15 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-740-15) / 1 CAPSULE in 1 BLISTER PACK (50268-740-11)

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": "41c4deb3-2dcf-b17a-e063-6294a90ad2be", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["62fa7fdf-c588-6f79-e053-2a91aa0a4c19"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX (50268-740-01)  / 1 CAPSULE in 1 BLISTER PACK (50268-740-11)", "package_ndc": "50268-740-01", "marketing_start_date": "20251022"}, {"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-740-15)  / 1 CAPSULE in 1 BLISTER PACK (50268-740-11)", "package_ndc": "50268-740-15", "marketing_start_date": "20180117"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "50268-740_41c4deb3-2dcf-b17a-e063-6294a90ad2be", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "50268-740", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA207405", "marketing_category": "ANDA", "marketing_start_date": "20180117", "listing_expiration_date": "20261231"}