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 CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

propranolol hydrochloride 80 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1501
Product ID 50090-1501_b566cbe1-2d29-4d46-bd9c-316e363c9174
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078703
Listing Expiration 2026-12-31
Marketing Start 2013-03-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901501
Hyphenated Format 50090-1501

Supplemental Identifiers

RxCUI
856569
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 ANDA078703 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0)
source: ndc

Packages (1)

50090-1501-0 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0)

Ingredients (1)

propranolol hydrochloride (80 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": "b566cbe1-2d29-4d46-bd9c-316e363c9174", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["d1cfdb57-0b04-43f7-bd10-c585f77385b3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-1501-0)", "package_ndc": "50090-1501-0", "marketing_start_date": "20141208"}], "brand_name": "propranolol hydrochloride", "product_id": "50090-1501_b566cbe1-2d29-4d46-bd9c-316e363c9174", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-1501", "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": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}