tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
chartwell rx, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-775
Product ID
62135-775_45adcea0-c5c1-9431-e063-6294a90a0471
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207405
Listing Expiration
2026-12-31
Marketing Start
2017-08-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135775
Hyphenated Format
62135-775
Supplemental Identifiers
RxCUI
UPC
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
ANDA207405 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (62135-775-30)
- 90 CAPSULE in 1 BOTTLE (62135-775-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45adcea0-c5c1-9431-e063-6294a90a0471", "openfda": {"upc": ["0362135775308", "0362135775902"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["14db58df-7584-410b-8cf4-4b928dada859"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62135-775-30)", "package_ndc": "62135-775-30", "marketing_start_date": "20231101"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62135-775-90)", "package_ndc": "62135-775-90", "marketing_start_date": "20230908"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "62135-775_45adcea0-c5c1-9431-e063-6294a90a0471", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "62135-775", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tamsulosin Hydrochloride", "active_ingredients": [{"name": "TAMSULOSIN HYDROCHLORIDE", "strength": ".4 mg/1"}], "application_number": "ANDA207405", "marketing_category": "ANDA", "marketing_start_date": "20170811", "listing_expiration_date": "20261231"}