tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler northwind health company, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-832
Product ID 51655-832_4973d0cd-3f6d-fb42-e063-6294a90a0882
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2027-12-31
Marketing Start 2022-02-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655832
Hyphenated Format 51655-832

Supplemental Identifiers

RxCUI
863669
UNII
11SV1951MR

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 ANDA202433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-26)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-52)
source: ndc

Packages (2)

51655-832-26 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-26) 51655-832-52 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-52)

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": "4973d0cd-3f6d-fb42-e063-6294a90a0882", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["d9df4fe0-90ab-0d96-e053-2a95a90a5ff1"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-26)", "package_ndc": "51655-832-26", "marketing_start_date": "20220923"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (51655-832-52)", "package_ndc": "51655-832-52", "marketing_start_date": "20220223"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "51655-832_4973d0cd-3f6d-fb42-e063-6294a90a0882", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "51655-832", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA202433", "marketing_category": "ANDA", "marketing_start_date": "20220223", "listing_expiration_date": "20271231"}