propranolol hydrochloride

Generic: propranolol hydrochloride

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name propranolol hydrochloride
Generic Name propranolol hydrochloride
Labeler atlantic biologicals corp.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

propranolol hydrochloride 20 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-8728
Product ID 17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9
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 178568728
Hyphenated Format 17856-8728

Supplemental Identifiers

RxCUI
856724
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 ANDA070979 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/5mL
source: ndc
Packaging
  • 50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP
source: ndc

Packages (1)

17856-8728-1 50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP

Ingredients (1)

propranolol hydrochloride (20 mg/5mL)

Linked Drug Pages (1)

Propranolol Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40333fbc-1ccd-7a2c-e063-6294a90a8bc9", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856724"], "spl_set_id": ["40333bee-749f-0b43-e063-6394a90a149c"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP in 1 CASE (17856-8728-1)  / 5 mL in 1 CUP", "package_ndc": "17856-8728-1", "marketing_start_date": "20251001"}], "brand_name": "Propranolol Hydrochloride", "product_id": "17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "17856-8728", "generic_name": "Propranolol Hydrochloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "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"}