tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

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

Drug Facts

Product Profile

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

tamsulosin hydrochloride .4 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7050
Product ID 68788-7050_574eb543-d5c6-4d15-a63c-7207e9d11745
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887050
Hyphenated Format 68788-7050

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
  • 100 CAPSULE in 1 BOTTLE (68788-7050-1)
  • 20 CAPSULE in 1 BOTTLE (68788-7050-2)
  • 30 CAPSULE in 1 BOTTLE (68788-7050-3)
  • 60 CAPSULE in 1 BOTTLE (68788-7050-6)
  • 120 CAPSULE in 1 BOTTLE (68788-7050-8)
  • 90 CAPSULE in 1 BOTTLE (68788-7050-9)
source: ndc

Packages (6)

68788-7050-1 100 CAPSULE in 1 BOTTLE (68788-7050-1) 68788-7050-2 20 CAPSULE in 1 BOTTLE (68788-7050-2) 68788-7050-3 30 CAPSULE in 1 BOTTLE (68788-7050-3) 68788-7050-6 60 CAPSULE in 1 BOTTLE (68788-7050-6) 68788-7050-8 120 CAPSULE in 1 BOTTLE (68788-7050-8) 68788-7050-9 90 CAPSULE in 1 BOTTLE (68788-7050-9)

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": "574eb543-d5c6-4d15-a63c-7207e9d11745", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["82d65964-de00-42c2-baaa-cc3de744b8eb"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68788-7050-1)", "package_ndc": "68788-7050-1", "marketing_start_date": "20200601"}, {"sample": false, "description": "20 CAPSULE in 1 BOTTLE (68788-7050-2)", "package_ndc": "68788-7050-2", "marketing_start_date": "20200601"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-7050-3)", "package_ndc": "68788-7050-3", "marketing_start_date": "20200601"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68788-7050-6)", "package_ndc": "68788-7050-6", "marketing_start_date": "20200601"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (68788-7050-8)", "package_ndc": "68788-7050-8", "marketing_start_date": "20200601"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68788-7050-9)", "package_ndc": "68788-7050-9", "marketing_start_date": "20200601"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "68788-7050_574eb543-d5c6-4d15-a63c-7207e9d11745", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68788-7050", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Preferred 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": "20200601", "listing_expiration_date": "20261231"}