propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8620
Product ID 68788-8620_8c765672-66b8-44bb-8252-792d539e057b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070322
Listing Expiration 2026-12-31
Marketing Start 2024-04-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888620
Hyphenated Format 68788-8620

Supplemental Identifiers

RxCUI
856519
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 ANDA070322 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8620-1)
  • 30 TABLET in 1 BOTTLE (68788-8620-3)
  • 60 TABLET in 1 BOTTLE (68788-8620-6)
  • 90 TABLET in 1 BOTTLE (68788-8620-9)
source: ndc

Packages (4)

68788-8620-1 100 TABLET in 1 BOTTLE (68788-8620-1) 68788-8620-3 30 TABLET in 1 BOTTLE (68788-8620-3) 68788-8620-6 60 TABLET in 1 BOTTLE (68788-8620-6) 68788-8620-9 90 TABLET in 1 BOTTLE (68788-8620-9)

Ingredients (1)

propranolol hydrochloride (40 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": "8c765672-66b8-44bb-8252-792d539e057b", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["52da1afc-7f1c-4893-ab84-8479dd939951"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8620-1)", "package_ndc": "68788-8620-1", "marketing_start_date": "20240402"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8620-3)", "package_ndc": "68788-8620-3", "marketing_start_date": "20240402"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8620-6)", "package_ndc": "68788-8620-6", "marketing_start_date": "20240402"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8620-9)", "package_ndc": "68788-8620-9", "marketing_start_date": "20240402"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68788-8620_8c765672-66b8-44bb-8252-792d539e057b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8620", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20240402", "listing_expiration_date": "20261231"}