NDC codes

FDA NDC Directory
Product NDC (as listed)71610-988Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0988Add 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
71610-988-307161009883030 TABLET in 1 BOTTLE (71610-988-30)Marketed from Feb 6, 2026
71610-988-457161009884545 TABLET in 1 BOTTLE (71610-988-45)Marketed from Feb 6, 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 71610-988_4a2baf2b-9abf-e333-e063-6294a90a110cSPL ID 4a2baf2b-9abf-e333-e063-6294a90a110cSPL set ID 4a2bba2d-9b7a-f43a-e063-6294a90af80eRxCUI 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

N471610098830 followed by a unit qualifier and the quantity

Package 71610-0988-30. 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)

Amlodipine besylate tablets is a calcium channel blocker and may be used alone or in combination with other antihypertensive and antianginal agents for the treatment of: Hypertension (1.1) Amlodipine besylate tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. Coronary Artery Disease (1.2) Chronic Stable Angina Vasospastic Angina (Prinzmetal’s or Variant Angina) Angiographically Documented Coronary Artery Disease in patients without heart failure or an ejection fraction < 40% 1.1 Hypertension Amlodipine besylate tablets are indicate…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-928
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-956
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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