tamsulosin hydrochloride
Generic: tamsulosin hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
tamsulosin hydrochloride
Generic Name
tamsulosin hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
tamsulosin hydrochloride .4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-947
Product ID
43063-947_415ef20a-0a9b-ddbc-e063-6294a90acdcb
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
43063947
Hyphenated Format
43063-947
Supplemental Identifiers
RxCUI
UPC
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, PLASTIC (43063-947-30)
- 90 CAPSULE in 1 BOTTLE, PLASTIC (43063-947-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415ef20a-0a9b-ddbc-e063-6294a90acdcb", "openfda": {"upc": ["0343063947906"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["f6b6aeab-bedd-4254-8811-4f65cf8a351f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-947-30)", "package_ndc": "43063-947-30", "marketing_start_date": "20190405"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (43063-947-90)", "package_ndc": "43063-947-90", "marketing_start_date": "20190214"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "43063-947_415ef20a-0a9b-ddbc-e063-6294a90acdcb", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "43063-947", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}