propranolol hydrochloride

Generic: propranolol hydrochloride

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

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-2078
Product ID 69238-2078_542e83a2-c56a-4910-b23c-8d1f4daabfc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071972
Listing Expiration 2026-12-31
Marketing Start 2021-06-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692382078
Hyphenated Format 69238-2078

Supplemental Identifiers

RxCUI
856448 856457 856519 856556 856578
UPC
0369238207811 0369238208016 0369238207910 0369238208115
UNII
F8A3652H1V

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 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
  • 100 TABLET in 1 BOTTLE (69238-2078-1)
  • 1000 TABLET in 1 BOTTLE (69238-2078-7)
source: ndc

Packages (2)

69238-2078-1 100 TABLET in 1 BOTTLE (69238-2078-1) 69238-2078-7 1000 TABLET in 1 BOTTLE (69238-2078-7)

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": "542e83a2-c56a-4910-b23c-8d1f4daabfc6", "openfda": {"upc": ["0369238207811", "0369238208016", "0369238207910", "0369238208115"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["14d0c95d-418f-40a8-bad3-e20c82424960"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69238-2078-1)", "package_ndc": "69238-2078-1", "marketing_start_date": "20210603"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69238-2078-7)", "package_ndc": "69238-2078-7", "marketing_start_date": "20210603"}], "brand_name": "Propranolol Hydrochloride", "product_id": "69238-2078_542e83a2-c56a-4910-b23c-8d1f4daabfc6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "69238-2078", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY 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": "20210603", "listing_expiration_date": "20261231"}