tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler st. mary's medical park pharmacy
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
St. Mary's Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-450
Product ID 60760-450_b96a08ae-b256-caca-e053-2995a90ab659
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204645
Listing Expiration 2026-12-31
Marketing Start 2021-01-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760450
Hyphenated Format 60760-450

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 ANDA204645 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (60760-450-90)
source: ndc

Packages (1)

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": "b96a08ae-b256-caca-e053-2995a90ab659", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["b969e0f3-1552-89d8-e053-2995a90acd7d"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (60760-450-90)", "package_ndc": "60760-450-90", "marketing_start_date": "20210122"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "60760-450_b96a08ae-b256-caca-e053-2995a90ab659", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60760-450", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "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": "20210122", "listing_expiration_date": "20261231"}