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 50090-7263
Product ID 50090-7263_152ccf8d-9d06-4ba2-bc76-ae5b11579d47
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212026
Listing Expiration 2026-12-31
Marketing Start 2020-01-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907263
Hyphenated Format 50090-7263

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 ANDA212026 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0)
source: ndc

Packages (1)

50090-7263-0 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0)

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": "152ccf8d-9d06-4ba2-bc76-ae5b11579d47", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["87967c3a-4a6e-45c8-ae3d-1e1dbaa4ba10"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7263-0)", "package_ndc": "50090-7263-0", "marketing_start_date": "20241003"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7263_152ccf8d-9d06-4ba2-bc76-ae5b11579d47", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7263", "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": "ANDA212026", "marketing_category": "ANDA", "marketing_start_date": "20200106", "listing_expiration_date": "20261231"}