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
71335-0398
Product ID
71335-0398_812a5db0-ce5b-47df-a7f9-ca14cdb1532b
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
713350398
Hyphenated Format
71335-0398
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 (71335-0398-1)
- 100 CAPSULE in 1 BOTTLE (71335-0398-2)
- 60 CAPSULE in 1 BOTTLE (71335-0398-3)
- 10 CAPSULE in 1 BOTTLE (71335-0398-4)
- 90 CAPSULE in 1 BOTTLE (71335-0398-5)
- 180 CAPSULE in 1 BOTTLE (71335-0398-6)
- 7 CAPSULE in 1 BOTTLE (71335-0398-7)
- 15 CAPSULE in 1 BOTTLE (71335-0398-8)
- 120 CAPSULE in 1 BOTTLE (71335-0398-9)
Packages (9)
71335-0398-1
30 CAPSULE in 1 BOTTLE (71335-0398-1)
71335-0398-2
100 CAPSULE in 1 BOTTLE (71335-0398-2)
71335-0398-3
60 CAPSULE in 1 BOTTLE (71335-0398-3)
71335-0398-4
10 CAPSULE in 1 BOTTLE (71335-0398-4)
71335-0398-5
90 CAPSULE in 1 BOTTLE (71335-0398-5)
71335-0398-6
180 CAPSULE in 1 BOTTLE (71335-0398-6)
71335-0398-7
7 CAPSULE in 1 BOTTLE (71335-0398-7)
71335-0398-8
15 CAPSULE in 1 BOTTLE (71335-0398-8)
71335-0398-9
120 CAPSULE in 1 BOTTLE (71335-0398-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "812a5db0-ce5b-47df-a7f9-ca14cdb1532b", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["58bdac81-680a-4fd2-8f05-dd5b86553569"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-0398-1)", "package_ndc": "71335-0398-1", "marketing_start_date": "20180425"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-0398-2)", "package_ndc": "71335-0398-2", "marketing_start_date": "20190111"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0398-3)", "package_ndc": "71335-0398-3", "marketing_start_date": "20180413"}, {"sample": false, "description": "10 CAPSULE in 1 BOTTLE (71335-0398-4)", "package_ndc": "71335-0398-4", "marketing_start_date": "20181108"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-0398-5)", "package_ndc": "71335-0398-5", "marketing_start_date": "20180413"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE (71335-0398-6)", "package_ndc": "71335-0398-6", "marketing_start_date": "20240405"}, {"sample": false, "description": "7 CAPSULE in 1 BOTTLE (71335-0398-7)", "package_ndc": "71335-0398-7", "marketing_start_date": "20181210"}, {"sample": false, "description": "15 CAPSULE in 1 BOTTLE (71335-0398-8)", "package_ndc": "71335-0398-8", "marketing_start_date": "20180611"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71335-0398-9)", "package_ndc": "71335-0398-9", "marketing_start_date": "20190722"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "71335-0398_812a5db0-ce5b-47df-a7f9-ca14cdb1532b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-0398", "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"}