NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1878Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1878Add 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
71335-1878-17133518780130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-1)Marketed from Aug 17, 2021
71335-1878-271335187802100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-2)Marketed from Sep 13, 2021
71335-1878-37133518780390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-3)Marketed from Jun 14, 2021
71335-1878-471335187804120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-4)Marketed from Sep 19, 2022
71335-1878-57133518780560 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-5)Marketed from Sep 19, 2022
71335-1878-671335187806180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-6)Marketed from Sep 19, 2022
71335-1878-77133518780710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-7)Marketed from Sep 19, 2022

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203894
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 71335-1878_123b5687-72fe-46ff-8902-472bc34b182fSPL ID 123b5687-72fe-46ff-8902-472bc34b182fSPL set ID a1997b48-8d66-437a-a253-ca996331b0c3RxCUI 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

N471335187801 followed by a unit qualifier and the quantity

Package 71335-1878-01. 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 .

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 myocardial …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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
ProductStrengthForm · routeLabelerProduct NDC
metoprolol succinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-567
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3122
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-663
metoprolol succinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralBryant Ranch Prepack63629-3286
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-566
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-564
metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralZydus Pharmaceuticals (USA) Inc.68382-565
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-5418
metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3164
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1875
metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralProficient Rx LP82804-198
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-1338
metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-1339
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-1340
metoprolol succinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralZydus Lifesciences Limited70771-1341
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC82868-083
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-5411
metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3143
Metoprolol Succinate ERMetoprolol succinate 50 mg/1Tablet, Extended releaseOralDirect_Rx72189-547
metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1951

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