phenoxybenzamine hydrochloride
Generic: phenoxybenzamine hydrochloride
Labeler: novitium pharma llcDrug Facts
Product Profile
Brand Name
phenoxybenzamine hydrochloride
Generic Name
phenoxybenzamine hydrochloride
Labeler
novitium pharma llc
Dosage Form
CAPSULE
Routes
Active Ingredients
phenoxybenzamine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70954-365
Product ID
70954-365_235c3c98-4dc2-4b5e-8bdc-f21d18cbb7ac
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215042
Listing Expiration
2026-12-31
Marketing Start
2022-07-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70954365
Hyphenated Format
70954-365
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
phenoxybenzamine hydrochloride (source: ndc)
Generic Name
phenoxybenzamine hydrochloride (source: ndc)
Application Number
ANDA215042 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (70954-365-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "235c3c98-4dc2-4b5e-8bdc-f21d18cbb7ac", "openfda": {"upc": ["0370954365105"], "unii": ["X1IEG24OHL"], "rxcui": ["861402"], "spl_set_id": ["2cb5fcd7-c37f-41de-8beb-0c7eded9ed04"], "manufacturer_name": ["Novitium Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70954-365-10)", "package_ndc": "70954-365-10", "marketing_start_date": "20220719"}], "brand_name": "Phenoxybenzamine Hydrochloride", "product_id": "70954-365_235c3c98-4dc2-4b5e-8bdc-f21d18cbb7ac", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70954-365", "generic_name": "Phenoxybenzamine Hydrochloride", "labeler_name": "Novitium Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenoxybenzamine Hydrochloride", "active_ingredients": [{"name": "PHENOXYBENZAMINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA215042", "marketing_category": "ANDA", "marketing_start_date": "20220719", "listing_expiration_date": "20261231"}