What is NDC 72189-547?

72189-547 is the product NDC for Metoprolol Succinate ER, Metoprolol succinate 50 mg/1 tablet, extended release, listed with the FDA by Direct_Rx. It has 1 package NDC, 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 Metoprolol Succinate ER?

2 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 ER NDC 72189-547

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-547Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0547Add 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
72189-547-90	7218905479072189054790	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-547-90)Marketed from Apr 11, 2024

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 ER
Generic name (nonproprietary): metoprolol succinate er
Active ingredients: Metoprolol succinate — 50 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203894
Marketing start: Apr 11, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 72189-547_15d5c223-af4f-e803-e063-6294a90af3d8SPL ID 15d5c223-af4f-e803-e063-6294a90af3d8SPL set ID 15d5c223-af4e-e803-e063-6294a90af3d8RxCUI 866436UNII TH25PD4CCB
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

N472189054790 followed by a unit qualifier and the quantity

Package 72189-0547-90. 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 Apr 11, 2024.

Indications (excerpt from the label)

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 myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including metoprolol. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to ac…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-547

What is NDC 72189-547?: 72189-547 is the product NDC for Metoprolol Succinate ER, Metoprolol succinate 50 mg/1 tablet, extended release, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metoprolol Succinate ER.
What is the active ingredient?: Metoprolol succinate.
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 Metoprolol Succinate ER?: 2 other product NDCs are listed under this name. See all Metoprolol Succinate ER 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 ER NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Metoprolol Succinate ER	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	DIrect_Rx	72189-652	72189-0652-90
Metoprolol Succinate ERmetoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Direct_Rx	61919-754	61919-0754-3061919-0754-90

Other NDCs under ANDA 203894

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

FDA NDC Directory listings under ANDA 203894
Product	Strength	Form · route	Labeler	Product NDC
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-5411
metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-5418
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	St Mary's Medical Park Pharmacy	60760-634
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	St. Mary's Medical Park Pharmacy	60760-663
metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	63629-3286
metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	Bryant Ranch Prepack	63629-9413
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Redpharm Drug	67296-1902
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-2522
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-2651
metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-564
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-565
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-566
metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	Zydus Pharmaceuticals (USA) Inc.	68382-567
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-3122
metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-3143
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-3164
metoprolol succinate	Metoprolol succinate 25 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1338
metoprolol succinate	Metoprolol succinate 50 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1339
metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1340
metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	Zydus Lifesciences Limited	70771-1341

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