Prescription drug · ANDA

Metoprolol Succinate NDC 82804-014

Metoprolol tartrate 50 mg/1 · Tablet, Extended release · Oral · Proficient Rx LP

NDC codes

FDA NDC Directory
Product NDC (as listed)82804-014Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0014Add 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 NDC11-digit (billing)PackageCopy
82804-014-30828040014308280400143030 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-30)Marketed from Oct 3, 2023
82804-014-60828040014608280400146060 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-60)Marketed from Oct 3, 2023
82804-014-90828040014908280400149090 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-90)Marketed from Oct 3, 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 tartrate — 50 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 82804
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207206
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 82804-014_502653e6-1971-4abf-9b21-ba0a9957672bSPL ID 502653e6-1971-4abf-9b21-ba0a9957672bSPL set ID 502653e6-1971-4abf-9b21-ba0a9957672bRxCUI 866436UNII W5S57Y3A5LUPC 0382804014903
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

N482804001430 followed by a unit qualifier and the quantity

Package 82804-0014-30. 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 .

Indications (excerpt from the label)

Metoprolol succinate extended-release tablets, metoprolol succinate, 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 is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primaril…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-014

What is NDC 82804-014?
82804-014 is the product NDC for Metoprolol Succinate, Metoprolol tartrate 50 mg/1 tablet, extended release, listed with the FDA by Proficient Rx LP. 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 tartrate.
Who is the labeler?
Proficient Rx LP, NDC labeler code 82804. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Metoprolol SuccinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralCoupler LLC67046-088367046-0883-03
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralCoupler LLC67046-168567046-1685-03
Metoprolol SuccinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralCoupler LLC67046-168667046-1686-03
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralOryza pharmaceuticals Inc.72516-02572516-0025-0172516-0025-1072516-0025-50
Metoprolol SuccinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-68468001-0684-0068001-0684-03
Metoprolol SuccinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-68568001-0685-0068001-0685-03
Metoprolol SuccinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-68668001-0686-0068001-0686-03
Metoprolol SuccinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralBluePoint Laboratories68001-68768001-0687-00
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralCoupler LLC67046-165067046-1650-03
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC53401-00953401-0009-3053401-0009-4553401-0009-53+3 more

All 251 Metoprolol Succinate NDCs

Other NDCs under ANDA 207206

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

FDA NDC Directory listings under ANDA 207206
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol SuccinateMetoprolol tartrate 100 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4190
Metoprolol SuccinateMetoprolol tartrate 50 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6448
Metoprolol SuccinateMetoprolol tartrate 25 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6488
Metoprolol SuccinateMetoprolol tartrate 25 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6489
Metoprolol SuccinateMetoprolol tartrate 50 mg/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-497
Metoprolol SuccinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralCranbury Pharmaceuticals, LLC27808-302
Metoprolol SuccinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralCranbury Pharmaceuticals, LLC27808-303
Metoprolol SuccinateMetoprolol tartrate 50 mg/1Tablet, Extended releaseOralNuCare Pharmaceuticals, Inc.68071-3943
Metoprolol SuccinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralCranbury Pharmaceuticals, LLC27808-304
Metoprolol SuccinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralCranbury Pharmaceuticals, LLC27808-305
Metoprolol SuccinateMetoprolol tartrate 50 mg/1Tablet, Extended releaseOralNuCare Pharmaceuticals, Inc.68071-3965
Metoprolol SuccinateMetoprolol tartrate 100 mg/1Tablet, Extended releaseOralOryza Pharmaceuticals, Inc72516-032
Metoprolol SuccinateMetoprolol tartrate 25 mg/1Tablet, Extended releaseOralOryza Pharmaceuticals, Inc72516-030
Metoprolol SuccinateMetoprolol tartrate 50 mg/1Tablet, Extended releaseOralOryza Pharmaceuticals, Inc72516-031
Metoprolol SuccinateMetoprolol tartrate 200 mg/1Tablet, Extended releaseOralOryza Pharmaceuticals, Inc72516-033
Metoprolol SuccinateMetoprolol tartrate 25 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4090
Metoprolol SuccinateMetoprolol tartrate 100 mg/1Tablet, Extended releaseOralPreferred Pharmaceuticals Inc68788-8448

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