Metoprolol Succinate NDC 67296-2125

NDC codes

FDA NDC Directory

Product NDC (as listed)67296-2125Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67296-2125Add 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 NDC	11-digit (billing)	Package
67296-2125-1	67296212501	7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2125-1)Marketed from Oct 2, 2023
67296-2125-3	67296212503	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2125-3)Marketed from Oct 2, 2023
67296-2125-6	67296212506	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-2125-6)Marketed from Oct 2, 2023

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 — 25 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Redpharm Drug
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216916
Marketing start: Oct 2, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 67296-2125_4ff1a0e3-1a63-2527-e063-6294a90ab8beSPL ID 4ff1a0e3-1a63-2527-e063-6294a90ab8beSPL set ID 301ec2ea-84cb-ad89-e063-6294a90af49dRxCUI 866427UNII TH25PD4CCBUPC 0370010782013, 0370010783010, 0370010781016
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

N467296212501 followed by a unit qualifier and the quantity

Package 67296-2125-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.