propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-423
Product ID 72789-423_3cf830d5-c282-64d5-e063-6294a90af427
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 72789423
Hyphenated Format 72789-423

Supplemental Identifiers

RxCUI
856457
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
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-423-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-423-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-423-90)
source: ndc

Packages (3)

72789-423-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-423-30) 72789-423-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-423-60) 72789-423-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-423-90)

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": "3cf830d5-c282-64d5-e063-6294a90af427", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["49d09308-74b0-4f9a-9c03-37234b5ee3a3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-423-30)", "package_ndc": "72789-423-30", "marketing_start_date": "20240712"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-423-60)", "package_ndc": "72789-423-60", "marketing_start_date": "20241223"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-423-90)", "package_ndc": "72789-423-90", "marketing_start_date": "20250603"}], "brand_name": "Propranolol Hydrochloride", "product_id": "72789-423_3cf830d5-c282-64d5-e063-6294a90af427", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-423", "generic_name": "Propranolol Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}