NDC codes

FDA NDC Directory
Product NDC (as listed)71610-928Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0928Add 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
71610-928-307161009283030 TABLET in 1 BOTTLE (71610-928-30)Marketed from Jul 23, 2025
71610-928-457161009284545 TABLET in 1 BOTTLE (71610-928-45)Marketed from Jul 23, 2025
71610-928-537161009285360 TABLET in 1 BOTTLE (71610-928-53)Marketed from Jul 23, 2025
71610-928-607161009286090 TABLET in 1 BOTTLE (71610-928-60)Marketed from Jan 23, 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)
Amlodipine Besylate
Generic name (nonproprietary)
amlodipine besylate
Active ingredients
Amlodipine besylate — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076719
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 71610-928_4910735f-515a-6896-e063-6294a90a3e7cSPL ID 4910735f-515a-6896-e063-6294a90a3e7cSPL set ID 3ab4ad3d-7795-058a-e063-6294a90abc86RxCUI 308135UNII 864V2Q084H
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel 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

N471610092830 followed by a unit qualifier and the quantity

Package 71610-0928-30. 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

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

Other NDCs under ANDA 076719

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

FDA NDC Directory listings under ANDA 076719
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-956
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-988
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralGSMS, Incorporated51407-950
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-514
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralGSMS, Incorporated51407-951
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-515
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-516

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