Prescription drug · ANDA

Metoprolol succinate NDC 72516-025

Metoprolol succinate 25 mg/1 · Tablet, Extended release · Oral · Oryza pharmaceuticals Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)72516-025Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72516-0025Add 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
72516-025-0172516002501100 TABLET, EXTENDED RELEASE in 1 PACKAGE (72516-025-01)Marketed from May 15, 2026
72516-025-10725160025101000 TABLET, EXTENDED RELEASE in 1 PACKAGE (72516-025-10)Marketed from May 15, 2026
72516-025-5072516002550500 TABLET, EXTENDED RELEASE in 1 PACKAGE (72516-025-50)Marketed from May 15, 2026

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 — 25 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 72516-025_5b7d4c2a-8577-3afc-e063-6394a90adbcaSPL ID 5b7d4c2a-8577-3afc-e063-6394a90adbca
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

N472516002501 followed by a unit qualifier and the quantity

Package 72516-0025-01. 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

The FDA listing for this product does not reference a label (SPL) set.

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 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
Metoprolol succinateMetoprolol succinate 100 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-3167

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Metoprolol succinate NDC 72516-025 | Med-Code