tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-160
Product ID 62756-160_52595417-3e2e-4d58-9167-dd5b2bf1b082
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090931
Listing Expiration 2026-12-31
Marketing Start 2010-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756160
Hyphenated Format 62756-160

Supplemental Identifiers

RxCUI
863669
UPC
0362756160811
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 ANDA090931 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (62756-160-08)
  • 500 CAPSULE in 1 BOTTLE (62756-160-13)
  • 1000 CAPSULE in 1 BOTTLE (62756-160-18)
  • 90 CAPSULE in 1 BOTTLE (62756-160-81)
  • 30 CAPSULE in 1 BOTTLE (62756-160-83)
  • 100 CAPSULE in 1 BOTTLE (62756-160-88)
source: ndc

Packages (6)

62756-160-08 100 CAPSULE in 1 BOTTLE (62756-160-08) 62756-160-13 500 CAPSULE in 1 BOTTLE (62756-160-13) 62756-160-18 1000 CAPSULE in 1 BOTTLE (62756-160-18) 62756-160-81 90 CAPSULE in 1 BOTTLE (62756-160-81) 62756-160-83 30 CAPSULE in 1 BOTTLE (62756-160-83) 62756-160-88 100 CAPSULE in 1 BOTTLE (62756-160-88)

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": "52595417-3e2e-4d58-9167-dd5b2bf1b082", "openfda": {"upc": ["0362756160811"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["d742707b-4c17-4b08-a9d0-491ba2bf6415"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-160-08)", "package_ndc": "62756-160-08", "marketing_start_date": "20100715"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (62756-160-13)", "package_ndc": "62756-160-13", "marketing_start_date": "20100715"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62756-160-18)", "package_ndc": "62756-160-18", "marketing_start_date": "20100715"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62756-160-81)", "package_ndc": "62756-160-81", "marketing_start_date": "20100715"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62756-160-83)", "package_ndc": "62756-160-83", "marketing_start_date": "20100715"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-160-88)", "package_ndc": "62756-160-88", "marketing_start_date": "20100715"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "62756-160_52595417-3e2e-4d58-9167-dd5b2bf1b082", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "62756-160", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090931", "marketing_category": "ANDA", "marketing_start_date": "20100715", "listing_expiration_date": "20261231"}