NDC codes

FDA NDC Directory
Product NDC (as listed)10631-010Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10631-0010Add 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
10631-010-301063100103030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-010-30)Marketed from Mar 15, 2018

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)
Kapspargo
Generic name (nonproprietary)
metoprolol succinate
Active ingredients
Metoprolol succinate100 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 210428
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 10631-010_b982da20-735c-49d8-ad1f-6a831194db87SPL ID b982da20-735c-49d8-ad1f-6a831194db87SPL set ID 9cfa55b4-15c6-40f7-b6e5-41096ee51bfcRxCUI 1999031, 1999033, 1999035, 1999037, 2047766, 2047769, 2047772, 2047775UNII 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

N410631001030 followed by a unit qualifier and the quantity

Package 10631-0010-30. 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)

KAPSPARGO Sprinkle is a beta 1 -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 KAPSPARGO Sprinkle is 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 benefits have been seen in c

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 210428

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

FDA NDC Directory listings under NDA 210428
ProductStrengthForm · routeLabelerProduct NDC
Metoprolol SuccinateMetoprolol succinate 25 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries Inc.63304-008
Metoprolol SuccinateMetoprolol succinate 50 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries Inc.63304-009
Metoprolol SuccinateMetoprolol succinate 100 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries Inc.63304-010
Metoprolol SuccinateMetoprolol succinate 200 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries Inc.63304-011
Kapspargometoprolol succinateMetoprolol succinate 25 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.10631-008
Kapspargometoprolol succinateMetoprolol succinate 50 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.10631-009
Kapspargometoprolol succinateMetoprolol succinate 200 mg/1Capsule, Extended releaseOralSun Pharmaceutical Industries, Inc.10631-011

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