phenoxybenzamine hydrochloride

Generic: phenoxybenzamine hydrochloride

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phenoxybenzamine hydrochloride
Generic Name phenoxybenzamine hydrochloride
Labeler amneal pharmaceuticals ny llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

phenoxybenzamine hydrochloride 10 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 60219-1502
Product ID 60219-1502_f872082d-e917-4945-9cd8-59c082cd32d8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212568
Listing Expiration 2026-12-31
Marketing Start 2020-10-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 602191502
Hyphenated Format 60219-1502

Supplemental Identifiers

RxCUI
861402
UNII
X1IEG24OHL

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 phenoxybenzamine hydrochloride (source: ndc)
Generic Name phenoxybenzamine hydrochloride (source: ndc)
Application Number ANDA212568 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (60219-1502-1)
source: ndc

Packages (1)

Ingredients (1)

phenoxybenzamine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f872082d-e917-4945-9cd8-59c082cd32d8", "openfda": {"unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["0be6a394-cd10-42fc-97cf-ad53d81d8d93"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (60219-1502-1)", "package_ndc": "60219-1502-1", "marketing_start_date": "20201030"}], "brand_name": "Phenoxybenzamine hydrochloride", "product_id": "60219-1502_f872082d-e917-4945-9cd8-59c082cd32d8", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60219-1502", "generic_name": "Phenoxybenzamine hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenoxybenzamine hydrochloride", "active_ingredients": [{"name": "PHENOXYBENZAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA212568", "marketing_category": "ANDA", "marketing_start_date": "20201030", "listing_expiration_date": "20261231"}