What is NDC 72603-143?

72603-143 is the product NDC for Metoprolol succinate, Metoprolol succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Northstar Rx LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Northstar Rx LLC, NDC labeler code 72603. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Metoprolol succinate?

250 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metoprolol succinate NDC 72603-143

NDC codes

FDA NDC Directory

Product NDC (as listed)72603-143Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72603-0143Add 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
72603-143-01	7260301430172603014301	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-01)Marketed from Apr 10, 2023
72603-143-02	7260301430272603014302	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-02)Marketed from Apr 10, 2023
72603-143-03	7260301430372603014303	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-143-03)Marketed from Sep 12, 2023

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): Metoprolol succinate
Generic name (nonproprietary): metoprolol succinate
Active ingredients: Metoprolol succinate — 50 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Northstar Rx LLCNDC labeler code 72603
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090617
Marketing start: Apr 10, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 72603-143_82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3SPL ID 82de0ba4-1cc6-e9d1-7dc3-844ff6ec1fb3SPL set ID ad097646-cc77-8d67-5974-cc00060409f2RxCUI 866427, 866436UNII TH25PD4CCBUPC 0372603143010, 0372603142013
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

N472603014301 followed by a unit qualifier and the quantity

Package 72603-0143-01. 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

Current FDA label (SPL), effective Jul 16, 2025.

Indications (excerpt from the label)

Metoprolol succinate extended-release tablets are a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Angina Pectoris. ( 1.2 ) Heart Failure, to reduce the risk of cardiovascular mortality and heart failure hospitalizations in patients with heart failure. ( 1.3) 1.1 Hypertension Metoprolol succinate extended-release tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocar…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72603-143

What is NDC 72603-143?: 72603-143 is the product NDC for Metoprolol succinate, Metoprolol succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Northstar Rx LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoprolol succinate.
What is the active ingredient?: Metoprolol succinate.
Who is the labeler?: Northstar Rx LLC, NDC labeler code 72603. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metoprolol succinate?: 250 other product NDCs are listed under this name. See all Metoprolol succinate 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 Metoprolol succinate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-0883	67046-0883-03
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1685	67046-1685-03
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1686	67046-1686-03
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Oryza pharmaceuticals Inc.	72516-025	72516-0025-0172516-0025-1072516-0025-50
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-684	68001-0684-0068001-0684-03
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-685	68001-0685-0068001-0685-03
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-686	68001-0686-0068001-0686-03
Metoprolol Succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-687	68001-0687-00
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Coupler LLC	67046-1650	67046-1650-03
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-009	53401-0009-3053401-0009-4553401-0009-53+3 more

All 251 Metoprolol succinate NDCs

Other NDCs under ANDA 090617

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

FDA NDC Directory listings under ANDA 090617
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-010
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-009
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceutcals, Inc.	68071-3828
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-7280
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-0149
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	71335-0158
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-2642
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Northstar Rx LLC	72603-142
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7118
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7117
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-540
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-7823
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-541
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	43063-624
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-7824
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Inc	75907-347
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Inc	75907-344
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6322
Metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6323
Metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Quallent Pharmaceuticals Health LLC	82009-113

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