What is NDC 82868-084?

82868-084 is the product NDC for Metoprolol Succinate, Metoprolol succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Northwind Health Company, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Northwind Health Company, LLC, NDC labeler code 82868. 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 82868-084

NDC codes

FDA NDC Directory

Product NDC (as listed)82868-084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82868-0084Add 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
82868-084-30	8286800843082868008430	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-30)Marketed from Aug 26, 2025
82868-084-90	8286800849082868008490	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-90)Marketed from Jun 25, 2025

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: Northwind Health Company, LLCNDC labeler code 82868
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216916
Marketing start: Jun 25, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 82868-084_471bdf68-b863-096f-e063-6294a90a84d1SPL ID 471bdf68-b863-096f-e063-6294a90a84d1SPL set ID 471bdbd7-7435-6786-e063-6294a90aa8a0RxCUI 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

N482868008430 followed by a unit qualifier and the quantity

Package 82868-0084-30. 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 Dec 29, 2025.

Indications (excerpt from the label)

Metoprolol succinate is 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 myocardial infarctions. These …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82868-084

What is NDC 82868-084?: 82868-084 is the product NDC for Metoprolol Succinate, Metoprolol succinate 50 mg/1 tablet, film coated, extended release, listed with the FDA by Northwind Health Company, LLC. It has 2 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?: Northwind Health Company, LLC, NDC labeler code 82868. 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 216916

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

FDA NDC Directory listings under ANDA 216916
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-7590
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	A-S Medication Solutions	50090-7591
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Redpharm Drug	67296-2125
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	NuCare Pharmaceuticals,Inc.	68071-3963
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-4022
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Preferred Pharmaceuticals Inc.	68788-8869
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-780
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-781
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-782
Metoprolol Succinate	Metoprolol succinate 200 mg/1	Tablet, Film coated, Extended releaseOral	Granules Pharmaceuticals Inc.	70010-783
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-4531
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-4533
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2592
Metoprolol Succinate	Metoprolol succinate 200 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2811
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-2945
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	71335-3052
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-576
Metoprolol Succinate	Metoprolol succinate 25 mg/1	Tablet, Film coated, Extended releaseOral	Proficient Rx LP	82804-262
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Proficient Rx LP	82804-279
Metoprolol Succinate	Metoprolol succinate 50 mg/1	Tablet, Film coated, Extended releaseOral	Proficient Rx LP	82804-301

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