tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1784
Product ID
71335-1784_a01182b6-3e16-4eb9-aa9c-b7b445b87709
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202433
Listing Expiration
2026-12-31
Marketing Start
2013-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351784
Hyphenated Format
71335-1784
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- .4 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71335-1784-1)
- 100 CAPSULE in 1 BOTTLE (71335-1784-2)
- 60 CAPSULE in 1 BOTTLE (71335-1784-3)
- 10 CAPSULE in 1 BOTTLE (71335-1784-4)
- 90 CAPSULE in 1 BOTTLE (71335-1784-5)
- 180 CAPSULE in 1 BOTTLE (71335-1784-6)
- 7 CAPSULE in 1 BOTTLE (71335-1784-7)
- 15 CAPSULE in 1 BOTTLE (71335-1784-8)
- 120 CAPSULE in 1 BOTTLE (71335-1784-9)
Packages (9)
71335-1784-1
30 CAPSULE in 1 BOTTLE (71335-1784-1)
71335-1784-2
100 CAPSULE in 1 BOTTLE (71335-1784-2)
71335-1784-3
60 CAPSULE in 1 BOTTLE (71335-1784-3)
71335-1784-4
10 CAPSULE in 1 BOTTLE (71335-1784-4)
71335-1784-5
90 CAPSULE in 1 BOTTLE (71335-1784-5)
71335-1784-6
180 CAPSULE in 1 BOTTLE (71335-1784-6)
71335-1784-7
7 CAPSULE in 1 BOTTLE (71335-1784-7)
71335-1784-8
15 CAPSULE in 1 BOTTLE (71335-1784-8)
71335-1784-9
120 CAPSULE in 1 BOTTLE (71335-1784-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a01182b6-3e16-4eb9-aa9c-b7b445b87709", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["59d0e07c-0018-4681-beb2-cb1c8e2637ee"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-1784-1)", "package_ndc": "71335-1784-1", "marketing_start_date": "20210310"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-1784-2)", "package_ndc": "71335-1784-2", "marketing_start_date": "20210310"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-1784-3)", "package_ndc": "71335-1784-3", "marketing_start_date": "20210310"}, {"sample": false, "description": "10 CAPSULE in 1 BOTTLE (71335-1784-4)", "package_ndc": "71335-1784-4", "marketing_start_date": "20210310"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-1784-5)", "package_ndc": "71335-1784-5", "marketing_start_date": "20210310"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE (71335-1784-6)", "package_ndc": "71335-1784-6", "marketing_start_date": "20210310"}, {"sample": false, "description": "7 CAPSULE in 1 BOTTLE (71335-1784-7)", "package_ndc": "71335-1784-7", "marketing_start_date": "20210310"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71335-1784-8)", "package_ndc": "71335-1784-8", "marketing_start_date": "20210310"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71335-1784-9)", "package_ndc": "71335-1784-9", "marketing_start_date": "20210310"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "71335-1784_a01182b6-3e16-4eb9-aa9c-b7b445b87709", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1784", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}