propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler st. mary's medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-731
Product ID 60760-731_42def69e-9eb7-af05-e063-6394a90a421c
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 60760731
Hyphenated Format 60760-731

Supplemental Identifiers

RxCUI
856457
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
  • 20 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60)
source: ndc

Packages (1)

60760-731-60 60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60)

Ingredients (1)

propranolol hydrochloride (20 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": "42def69e-9eb7-af05-e063-6394a90a421c", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["42def694-9484-a2ca-e063-6394a90a87d8"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60)", "package_ndc": "60760-731-60", "marketing_start_date": "20251105"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60760-731_42def69e-9eb7-af05-e063-6394a90a421c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-731", "generic_name": "Propranolol Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}