propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7104
Product ID 50090-7104_1d38c2d9-7c4a-4449-b0d5-55131d43f3cb
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 500907104
Hyphenated Format 50090-7104

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 ANDA071972 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (50090-7104-1)
  • 90 TABLET in 1 BOTTLE (50090-7104-6)
source: ndc

Packages (2)

50090-7104-1 60 TABLET in 1 BOTTLE (50090-7104-1) 50090-7104-6 90 TABLET in 1 BOTTLE (50090-7104-6)

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": "1d38c2d9-7c4a-4449-b0d5-55131d43f3cb", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["7b751df5-0751-435b-8755-3d50476cabd2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7104-1)", "package_ndc": "50090-7104-1", "marketing_start_date": "20240229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7104-6)", "package_ndc": "50090-7104-6", "marketing_start_date": "20240229"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7104_1d38c2d9-7c4a-4449-b0d5-55131d43f3cb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7104", "generic_name": "Propranolol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}