NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0149Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0149Add 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
71335-0149-17133501490130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-1)Marketed from Jan 28, 2014
71335-0149-271335014902100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-2)Marketed from Jan 28, 2014
71335-0149-37133501490390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-3)Marketed from Jan 28, 2014
71335-0149-471335014904120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-4)Marketed from Jan 28, 2014
71335-0149-57133501490560 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0149-5)Marketed from Jan 28, 2014

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 090617
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 71335-0149_609cf08a-a8d7-4e20-83e6-05823fb89286SPL ID 609cf08a-a8d7-4e20-83e6-05823fb89286SPL set ID 42bb324d-8b1e-45db-b15e-3845eec83c38RxCUI 866427, 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

N471335014901 followed by a unit qualifier and the quantity

Package 71335-0149-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Metoprolol succinate extended-release tablets, metoprolol succinate, is a beta 1 -selective adrenoceptor blocking agent. Metoprolol succinate extended-release tablets are 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 - for the treatment of stable, symptomatic (NYHA Class II or III) heart failure of ischemic, hypertensive, or cardiomyopathic origin.( 1.3) 1.1 Hypertension Metoprolol succinate extended-release tablets are indicated for the treatment of hypertension, to lower blood pressure. Lo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 090617

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

FDA NDC Directory listings under ANDA 090617
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7823
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-7824
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-284
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralAvPAK50268-541
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralAvPAK50268-540
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralMajor Pharmaceuticals0904-6323
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralQuallent Pharmaceuticals Health LLC82009-113
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralQuallent Pharmaceuticals Health LLC82009-114
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-7117
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-7118
Metoprolol SuccinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralCardinal Health 107, LLC55154-4698
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralDr. Reddy's Laboratories Limited55111-466
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralNorthstar Rx LLC72603-142
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralDr. Reddy's Laboratories Limited55111-467
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralMajor Pharmaceuticals0904-6322
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralNorthstar Rx LLC72603-143
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralPD-Rx Pharmaceuticals, Inc.43063-624
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-7238
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-7239
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Film coated, Extended releaseOralDr. Reddy's Laboratories Inc75907-344

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