Propranolol Hydrochloride NDC 17856-8728

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-8728Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-8728Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
17856-8728-1	17856872801	50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUPMarketed from Oct 1, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Propranolol Hydrochloride
Generic name (nonproprietary): propranolol hydrochloride
Active ingredients: Propranolol hydrochloride — 20 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: ATLANTIC BIOLOGICALS CORP.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070979
Marketing start: May 15, 1987
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9SPL ID 40333fbc-1ccd-7a2c-e063-6294a90a8bc9SPL set ID 40333bee-749f-0b43-e063-6394a90a149cRxCUI 856724UNII F8A3652H1V
Pharmacologic class: beta-Adrenergic Blocker

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N417856872801 followed by a unit qualifier and the quantity

Package 17856-8728-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 070979

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 070979
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	ATLANTIC BIOLOGICALS CORP.	17856-3728
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	Pharmaceutical Associates, Inc.	0121-0908