propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2372
Product ID 71335-2372_b087d364-8bf6-4326-9cfa-8e3c79f09edb
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 713352372
Hyphenated Format 71335-2372

Supplemental Identifiers

RxCUI
856448
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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-2372-1)
  • 60 TABLET in 1 BOTTLE (71335-2372-2)
  • 100 TABLET in 1 BOTTLE (71335-2372-3)
  • 90 TABLET in 1 BOTTLE (71335-2372-4)
  • 120 TABLET in 1 BOTTLE (71335-2372-5)
  • 10 TABLET in 1 BOTTLE (71335-2372-6)
source: ndc

Packages (6)

71335-2372-1 30 TABLET in 1 BOTTLE (71335-2372-1) 71335-2372-2 60 TABLET in 1 BOTTLE (71335-2372-2) 71335-2372-3 100 TABLET in 1 BOTTLE (71335-2372-3) 71335-2372-4 90 TABLET in 1 BOTTLE (71335-2372-4) 71335-2372-5 120 TABLET in 1 BOTTLE (71335-2372-5) 71335-2372-6 10 TABLET in 1 BOTTLE (71335-2372-6)

Ingredients (1)

propranolol hydrochloride (10 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": "b087d364-8bf6-4326-9cfa-8e3c79f09edb", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["a21eb31b-db50-47a5-8f4c-315c2a842c8b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2372-1)", "package_ndc": "71335-2372-1", "marketing_start_date": "20240529"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2372-2)", "package_ndc": "71335-2372-2", "marketing_start_date": "20240529"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2372-3)", "package_ndc": "71335-2372-3", "marketing_start_date": "20240529"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2372-4)", "package_ndc": "71335-2372-4", "marketing_start_date": "20240529"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2372-5)", "package_ndc": "71335-2372-5", "marketing_start_date": "20240529"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2372-6)", "package_ndc": "71335-2372-6", "marketing_start_date": "20240529"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71335-2372_b087d364-8bf6-4326-9cfa-8e3c79f09edb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2372", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}