propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

propranolol hydrochloride 1 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1338
Product ID 51662-1338_37b5006f-2441-f90b-e063-6294a90abb12
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077760
Listing Expiration 2026-12-31
Marketing Start 2018-12-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621338
Hyphenated Format 51662-1338

Supplemental Identifiers

RxCUI
856443
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 ANDA077760 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL (51662-1338-1)
  • 10 POUCH in 1 CASE (51662-1338-3) / 1 VIAL in 1 POUCH (51662-1338-2) / 1 mL in 1 VIAL
source: ndc

Packages (2)

Ingredients (1)

propranolol hydrochloride (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "37b5006f-2441-f90b-e063-6294a90abb12", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["7da73cee-4e98-462d-e053-2991aa0a8bf4"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1338-1)", "package_ndc": "51662-1338-1", "marketing_start_date": "20181222"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1338-3)  / 1 VIAL in 1 POUCH (51662-1338-2)  / 1 mL in 1 VIAL", "package_ndc": "51662-1338-3", "marketing_start_date": "20221001"}], "brand_name": "PROPRANOLOL HYDROCHLORIDE", "product_id": "51662-1338_37b5006f-2441-f90b-e063-6294a90abb12", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1338", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPRANOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA077760", "marketing_category": "ANDA", "marketing_start_date": "20181222", "listing_expiration_date": "20261231"}