propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler hikma pharmaceuticals usa inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/5mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-3727
Product ID 0054-3727_245a43cc-cbf8-486d-ad3c-724aca63fd72
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070979
Listing Expiration 2026-12-31
Marketing Start 1987-05-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00543727
Hyphenated Format 0054-3727

Supplemental Identifiers

RxCUI
856724 856733
UPC
0300543730632 0300543727632
UNII
F8A3652H1V

Packaging Origin

Original Packager
true

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 ANDA070979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/5mL
source: ndc
Packaging
  • 500 mL in 1 BOTTLE, PLASTIC (0054-3727-63)
source: ndc

Packages (1)

Ingredients (1)

propranolol hydrochloride (20 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "245a43cc-cbf8-486d-ad3c-724aca63fd72", "openfda": {"upc": ["0300543730632", "0300543727632"], "unii": ["F8A3652H1V"], "rxcui": ["856724", "856733"], "spl_set_id": ["8fe0a04c-bf5b-4ba0-9df6-58c27f24b52e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (0054-3727-63)", "package_ndc": "0054-3727-63", "marketing_start_date": "19870515"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0054-3727_245a43cc-cbf8-486d-ad3c-724aca63fd72", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0054-3727", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA070979", "marketing_category": "ANDA", "marketing_start_date": "19870515", "listing_expiration_date": "20261231"}