What is NDC 72189-322?

72189-322 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 10 mg/1 tablet, listed with the FDA by Direct Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.

Direct Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Propranolol Hydrochloride?

196 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Propranolol Hydrochloride NDC 72189-322

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0322Add 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
72189-322-30	7218903223072189032230	30 TABLET in 1 BOTTLE (72189-322-30)Marketed from Feb 11, 2022
72189-322-60	7218903226072189032260	60 TABLET in 1 BOTTLE (72189-322-60)Marketed from Feb 11, 2022
72189-322-90	7218903229072189032290	90 TABLET in 1 BOTTLE (72189-322-90)Marketed from Feb 11, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Direct RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 070322
Marketing start: Feb 11, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 72189-322_2c3d2dfe-1000-b986-e063-6294a90a84c9SPL ID 2c3d2dfe-1000-b986-e063-6294a90a84c9SPL set ID d7c0cc12-6d2d-7146-e053-2995a90a85a4RxCUI 856448UNII 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

N472189032230 followed by a unit qualifier and the quantity

Package 72189-0322-30. 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

Current FDA label (SPL), effective Jan 21, 2025.

Indications (excerpt from the label)

Hypertension Propranolol hydrochloride tablets, USP are indicated in the management of hypertension. They may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride tablets, USP are not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride tablets, USP are indicated to decrease angina frequency and increase exercise tolerance in patients with angina pectoris. Atrial Fibrillation Propranolol hydrochloride tablets, USP are indicated to control ventricular rate in patients with atrial fibrillation and a rapid ventricular response. Myocardial …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-322

What is NDC 72189-322?: 72189-322 is the product NDC for Propranolol Hydrochloride, Propranolol hydrochloride 10 mg/1 tablet, listed with the FDA by Direct Rx. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Propranolol Hydrochloride.
What is the active ingredient?: Propranolol hydrochloride.
Who is the labeler?: Direct Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Propranolol Hydrochloride?: 196 other product NDCs are listed under this name. See all Propranolol Hydrochloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Propranolol Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	American Health Packaging	60687-948	60687-0948-01
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-132	82619-0132-0182619-0132-02
Propranolol Hydrochloride	Propranolol hydrochloride 80 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-133	82619-0133-0182619-0133-02
Propranolol Hydrochloride	Propranolol hydrochloride 120 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-134	82619-0134-0182619-0134-02
Propranolol Hydrochloride	Propranolol hydrochloride 160 mg/1	Capsule, Extended releaseOral	Creekwood Pharmaceuticals LLC	82619-135	82619-0135-0182619-0135-02
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0958	00121-0958-16
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/5mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-4958	00121-4958-40
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2584	55154-2584-00
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	American Health Packaging	60687-937	60687-0937-01
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0583	80425-0583-0180425-0583-0280425-0583-03

All 197 Propranolol Hydrochloride NDCs

Other NDCs under ANDA 070322

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

FDA NDC Directory listings under ANDA 070322
Product	Strength	Form · route	Labeler	Product NDC
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-426
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	Proficient Rx LP	71205-794
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1994
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-3102
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0464
Propranolol hydrochloride	Propranolol hydrochloride 80 mg/1	TabletOral	Bryant Ranch Prepack	71335-2594
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Proficient Rx LP	71205-590
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-987
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	American Health Packaging	60687-587
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	American Health Packaging	60687-598
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	American Health Packaging	60687-609
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-495
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4292
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8620
Propranolol Hydrochloride	Propranolol hydrochloride 10 mg/1	TabletOral	Asclemed USA, Inc.	76420-383
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-1712
Propranolol Hydrochloride	Propranolol hydrochloride 20 mg/1	TabletOral	Asclemed USA, Inc.	76420-384
Propranolol Hydrochloride	Propranolol hydrochloride 40 mg/1	TabletOral	Asclemed USA, Inc.	76420-385
Propranolol Hydrochloride	Propranolol hydrochloride 60 mg/1	TabletOral	Asclemed USA, Inc.	76420-386
Propranolol hydrochloride	Propranolol hydrochloride 80 mg/1	TabletOral	Asclemed USA, Inc.	76420-387

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