NDC codes

FDA NDC Directory
Product NDC (as listed)71335-3167Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-3167Add 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
71335-3167-17133531670130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-1)Marketed from Aug 4, 2026
71335-3167-27133531670290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-2)Marketed from Aug 4, 2026
71335-3167-371335316703120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-3)Marketed from Aug 4, 2026
71335-3167-47133531670420 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-4)Marketed from Aug 4, 2026
71335-3167-571335316705100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-5)Marketed from Aug 4, 2026
71335-3167-67133531670660 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-6)Marketed from Aug 4, 2026
71335-3167-77133531670710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-7)Marketed from Aug 4, 2026

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 — 100 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214110
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 71335-3167_ccca9f4b-3d0f-467a-a4a7-8505fae57d0eSPL ID ccca9f4b-3d0f-467a-a4a7-8505fae57d0eSPL set ID a693bef9-cdfa-4012-ac87-873b9c5bf1cdRxCUI 866412UNII 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

N471335316701 followed by a unit qualifier and the quantity

Package 71335-3167-01. 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, 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 b…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214110

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

FDA NDC Directory listings under ANDA 214110
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralCoupler LLC67046-1685
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralZhejiang Jutai Pharamceutical Co., Ltd71765-006
Metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralZhejiang Jutai Pharamceutical Co., Ltd71765-007
Metoprolol succinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralZhejiang Jutai Pharamceutical Co., Ltd71765-008
Metoprolol succinateMetoprolol succinate 25 mg/1Tablet, Extended releaseOralOryza pharmaceuticals Inc.72516-025
Metoprolol succinateMetoprolol succinate 50 mg/1Tablet, Extended releaseOralOryza pharmaceuticals Inc.72516-026
Metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralOryza pharmaceuticals Inc.72516-027
Metoprolol succinateMetoprolol succinate 200 mg/1Tablet, Extended releaseOralOryza pharmaceuticals Inc.72516-028

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