propranolol

Generic: propranolol hydrochloride

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol
Generic Name propranolol hydrochloride
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

propranolol hydrochloride 1 mg/mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-604
Product ID 84549-604_45b0aaf0-df6d-7db0-e063-6294a90a9135
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075826
Listing Expiration 2026-12-31
Marketing Start 2001-09-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549604
Hyphenated Format 84549-604

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 (source: ndc)
Generic Name propranolol hydrochloride (source: ndc)
Application Number ANDA075826 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL, SINGLE-DOSE (84549-604-01)
source: ndc

Packages (1)

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": "45b0aaf0-df6d-7db0-e063-6294a90a9135", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["45b0aaf0-df6c-7db0-e063-6294a90a9135"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-604-01)", "package_ndc": "84549-604-01", "marketing_start_date": "20251211"}], "brand_name": "Propranolol", "product_id": "84549-604_45b0aaf0-df6d-7db0-e063-6294a90a9135", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "84549-604", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075826", "marketing_category": "ANDA", "marketing_start_date": "20010907", "listing_expiration_date": "20261231"}