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 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7593
Product ID 50090-7593_f61eb97c-5511-46a7-a26c-d31405f337d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078955
Listing Expiration 2027-12-31
Marketing Start 2024-09-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907593
Hyphenated Format 50090-7593

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 ANDA078955 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-7593-1)
  • 90 TABLET in 1 BOTTLE (50090-7593-5)
source: ndc

Packages (2)

50090-7593-1 100 TABLET in 1 BOTTLE (50090-7593-1) 50090-7593-5 90 TABLET in 1 BOTTLE (50090-7593-5)

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": "f61eb97c-5511-46a7-a26c-d31405f337d3", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["1bb6d65a-8264-4fa4-92d4-c4a756ec49ea"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7593-1)", "package_ndc": "50090-7593-1", "marketing_start_date": "20250703"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7593-5)", "package_ndc": "50090-7593-5", "marketing_start_date": "20250703"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7593_f61eb97c-5511-46a7-a26c-d31405f337d3", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7593", "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": "10 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20271231"}