tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler ascend laboratories, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-450
Product ID 67877-450_6803a320-4e6f-4f1a-bfcf-955daf90fa76
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207405
Listing Expiration 2026-12-31
Marketing Start 2017-08-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877450
Hyphenated Format 67877-450

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 CAPSULE in 1 BOTTLE (67877-450-01)
  • 500 CAPSULE in 1 BOTTLE (67877-450-05)
  • 1000 CAPSULE in 1 BOTTLE (67877-450-10)
  • 30 CAPSULE in 1 BOTTLE (67877-450-30)
  • 10 BLISTER PACK in 1 CARTON (67877-450-38) / 10 CAPSULE in 1 BLISTER PACK (67877-450-33)
  • 60 CAPSULE in 1 BOTTLE (67877-450-60)
source: ndc

Packages (6)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6803a320-4e6f-4f1a-bfcf-955daf90fa76", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["ed9988bc-0759-4c36-bee1-11b68dc1c84c"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (67877-450-01)", "package_ndc": "67877-450-01", "marketing_start_date": "20170811"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (67877-450-05)", "package_ndc": "67877-450-05", "marketing_start_date": "20170811"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (67877-450-10)", "package_ndc": "67877-450-10", "marketing_start_date": "20170811"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (67877-450-30)", "package_ndc": "67877-450-30", "marketing_start_date": "20170811"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-450-38)  / 10 CAPSULE in 1 BLISTER PACK (67877-450-33)", "package_ndc": "67877-450-38", "marketing_start_date": "20170811"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (67877-450-60)", "package_ndc": "67877-450-60", "marketing_start_date": "20170811"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "67877-450_6803a320-4e6f-4f1a-bfcf-955daf90fa76", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "67877-450", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "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": "20170811", "listing_expiration_date": "20261231"}