propranolol
Generic: propranolol hydrochloride
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
propranolol
Generic Name
propranolol hydrochloride
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
propranolol hydrochloride 1 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549604
Hyphenated Format
84549-604
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 mL in 1 VIAL, SINGLE-DOSE (84549-604-01)
Packages (1)
Ingredients (1)
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"}