What is NDC 82009-116?

82009-116 is the product NDC for Metoprolol succinate, Metoprolol succinate 200 mg/1 tablet, film coated, extended release, listed with the FDA by Quallent Pharmaceuticals Health LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Quallent Pharmaceuticals Health LLC, NDC labeler code 82009. 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?

245 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 82009-116

NDC codes

FDA NDC Directory

Product NDC (as listed)82009-116Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82009-0116Add 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
82009-116-05	8200901160582009011605	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-116-05)Marketed from Jul 20, 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 — 200 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Quallent Pharmaceuticals Health LLCNDC labeler code 82009
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078889
Marketing start: Jul 20, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 82009-116_65151fb6-9d77-fb5b-bde1-8d78322e4a1aSPL ID 65151fb6-9d77-fb5b-bde1-8d78322e4a1aSPL set ID e147a897-4a23-1e1a-73cd-f2e6c9a7280dRxCUI 866412, 866419UNII TH25PD4CCBUPC 0382009116051, 0382009115054
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

N482009011605 followed by a unit qualifier and the quantity

Package 82009-0116-05. 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 82009-116

What is NDC 82009-116?: 82009-116 is the product NDC for Metoprolol succinate, Metoprolol succinate 200 mg/1 tablet, film coated, extended release, listed with the FDA by Quallent Pharmaceuticals Health LLC. It has 1 package NDC, 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?: Quallent Pharmaceuticals Health LLC, NDC labeler code 82009. 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?: 245 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 246 Metoprolol succinate NDCs

Other NDCs under ANDA 078889

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

FDA NDC Directory listings under ANDA 078889
Product	Strength	Form · route	Labeler	Product NDC
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-7825
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Major Pharmaceuticals	0904-6324
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	PD-Rx Pharmaceuticals, Inc.	43063-841
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7069
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-7070
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-542
Metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Film coated, Extended releaseOral	AvPAK	50268-543
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Aphena Pharma Solutions - Tennessee, LLC	53401-014
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Limited	55111-468
Metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Film coated, Extended releaseOral	Dr. Reddy's Laboratories Limited	55111-469
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-4347
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 107, LLC	55154-7279
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	American Health Packaging	60687-413
Metoprolol Succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Direct_Rx	61919-334
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	Proficient Rx LP	63187-768
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	Redpharm Drug	67296-2321
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-119
Metoprolol succinate	Metoprolol succinate 200 mg/1	Tablet, Extended releaseOral	BluePoint Laboratories	68001-120
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-2080
Metoprolol succinate	Metoprolol succinate 100 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-4456

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