propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler cardinal health 107, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-2646
Product ID 55154-2646_74dc9949-010c-4f2c-9aef-63ab466ba657
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071972
Listing Expiration 2026-12-31
Marketing Start 2025-02-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551542646
Hyphenated Format 55154-2646

Supplemental Identifiers

RxCUI
856457
UPC
0055154264600
UNII
F8A3652H1V

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 propranolol hydrochloride (source: ndc)
Generic Name propranolol hydrochloride (source: ndc)
Application Number ANDA071972 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-2646-0) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

55154-2646-0 10 BLISTER PACK in 1 BAG (55154-2646-0) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

propranolol hydrochloride (20 mg/1)

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "74dc9949-010c-4f2c-9aef-63ab466ba657", "openfda": {"upc": ["0055154264600"], "unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["74dc9949-010c-4f2c-9aef-63ab466ba657"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2646-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-2646-0", "marketing_start_date": "20250228"}], "brand_name": "Propranolol Hydrochloride", "product_id": "55154-2646_74dc9949-010c-4f2c-9aef-63ab466ba657", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55154-2646", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20250228", "listing_expiration_date": "20261231"}