tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-014
Product ID 57237-014_f89b21ae-6df5-4250-8034-92dd3b074ab9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202433
Listing Expiration 2027-12-31
Marketing Start 2013-04-30

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57237014
Hyphenated Format 57237-014

Supplemental Identifiers

RxCUI
863669
UPC
0357237014011
UNII
11SV1951MR

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (57237-014-01)
  • 500 CAPSULE in 1 BOTTLE (57237-014-05)
source: ndc

Packages (2)

57237-014-01 100 CAPSULE in 1 BOTTLE (57237-014-01) 57237-014-05 500 CAPSULE in 1 BOTTLE (57237-014-05)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/1)

Linked Drug Pages (1)

Tamsulosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f89b21ae-6df5-4250-8034-92dd3b074ab9", "openfda": {"upc": ["0357237014011"], "unii": ["11SV1951MR"], "rxcui": ["863669"], "spl_set_id": ["a242c8dc-576e-4a1f-a9e7-a05d7ebc0e0a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57237-014-01)", "package_ndc": "57237-014-01", "marketing_start_date": "20130430"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (57237-014-05)", "package_ndc": "57237-014-05", "marketing_start_date": "20130430"}], "brand_name": "Tamsulosin Hydrochloride", "product_id": "57237-014_f89b21ae-6df5-4250-8034-92dd3b074ab9", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "57237-014", "generic_name": "Tamsulosin Hydrochloride", "labeler_name": "Rising Pharma Holdings, 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": "20271231"}