propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler direct rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 10 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-074
Product ID 72189-074_2be818df-f32a-45a2-e063-6294a90a334a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070217
Listing Expiration 2026-12-31
Marketing Start 2020-06-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189074
Hyphenated Format 72189-074

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 ANDA070217 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-074-30)
source: ndc

Packages (1)

72189-074-30 30 TABLET in 1 BOTTLE (72189-074-30)

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": "2be818df-f32a-45a2-e063-6294a90a334a", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["a834d1cf-72fc-93bf-e053-2995a90a6191"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-074-30)", "package_ndc": "72189-074-30", "marketing_start_date": "20200616"}], "brand_name": "PROPRANOLOL HYDROCHLORIDE", "product_id": "72189-074_2be818df-f32a-45a2-e063-6294a90a334a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-074", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPRANOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070217", "marketing_category": "ANDA", "marketing_start_date": "20200616", "listing_expiration_date": "20261231"}