tamsulosin hydrochloride

Generic: tamsulosin hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tamsulosin hydrochloride
Generic Name tamsulosin hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

tamsulosin hydrochloride .4 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063947
Hyphenated Format 43063-947

Supplemental Identifiers

RxCUI
863669
UPC
0343063947906
UNII
11SV1951MR

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
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-947-30)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (43063-947-90)
source: ndc

Packages (2)

Ingredients (1)

tamsulosin hydrochloride (.4 mg/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"}