tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4443
Product ID 68071-4443_1a8cbdda-6567-1230-e063-6394a90a5083
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2026-12-31
Marketing Start 2013-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714443
Hyphenated Format 68071-4443

Supplemental Identifiers

RxCUI
863669
UPC
0368071444391
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
  • 10 CAPSULE in 1 BOTTLE (68071-4443-1)
  • 30 CAPSULE in 1 BOTTLE (68071-4443-3)
  • 60 CAPSULE in 1 BOTTLE (68071-4443-6)
  • 90 CAPSULE in 1 BOTTLE (68071-4443-9)
source: ndc

Packages (4)

68071-4443-1 10 CAPSULE in 1 BOTTLE (68071-4443-1) 68071-4443-3 30 CAPSULE in 1 BOTTLE (68071-4443-3) 68071-4443-6 60 CAPSULE in 1 BOTTLE (68071-4443-6) 68071-4443-9 90 CAPSULE in 1 BOTTLE (68071-4443-9)

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": "1a8cbdda-6567-1230-e063-6394a90a5083", "openfda": {"upc": ["0368071444391"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["6cb939a6-2bc6-5ca0-e053-2991aa0a4e69"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 CAPSULE in 1 BOTTLE (68071-4443-1)", "package_ndc": "68071-4443-1", "marketing_start_date": "20180521"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-4443-3)", "package_ndc": "68071-4443-3", "marketing_start_date": "20180521"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68071-4443-6)", "package_ndc": "68071-4443-6", "marketing_start_date": "20180521"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68071-4443-9)", "package_ndc": "68071-4443-9", "marketing_start_date": "20180521"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "68071-4443_1a8cbdda-6567-1230-e063-6394a90a5083", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4443", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20130430", "listing_expiration_date": "20261231"}