propranolol hydrochloride
Generic: propranolol hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
propranolol hydrochloride
Generic Name
propranolol hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
propranolol hydrochloride 20 mg/5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00543727
Hyphenated Format
0054-3727
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 20 mg/5mL
Packaging
- 500 mL in 1 BOTTLE, PLASTIC (0054-3727-63)
Packages (1)
Ingredients (1)
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"}