tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
avkare
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-989
Product ID
42291-989_43bec92e-7ee1-85d6-e063-6394a90a3167
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090377
Listing Expiration
2026-12-31
Marketing Start
2025-11-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291989
Hyphenated Format
42291-989
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA090377 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/1
Packaging
- 1000 CAPSULE in 1 BOTTLE (42291-989-10)
- 90 CAPSULE in 1 BOTTLE (42291-989-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43bec92e-7ee1-85d6-e063-6394a90a3167", "openfda": {"unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["43bec742-fbc4-39af-e063-6294a90ac734"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (42291-989-10)", "package_ndc": "42291-989-10", "marketing_start_date": "20251116"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (42291-989-90)", "package_ndc": "42291-989-90", "marketing_start_date": "20251116"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "42291-989_43bec92e-7ee1-85d6-e063-6394a90a3167", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "42291-989", "generic_name": "TAMSULOSIN HYDROCHLORIDE", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA090377", "marketing_category": "ANDA", "marketing_start_date": "20251116", "listing_expiration_date": "20261231"}