NDC codes

FDA NDC Directory
Product NDC (as listed)64980-725Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64980-0725Add 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
64980-725-09649800725096498007250990 TABLET in 1 BOTTLE (64980-725-09)Marketed from Jul 20, 2026
64980-725-1064980072510649800725101000 TABLET in 1 BOTTLE (64980-725-10)Marketed from Jul 20, 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
Labeler
Rising Pharma Holdings, Inc.NDC labeler code 64980
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 201380
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 64980-725_01b46020-bf09-4338-9dd9-c0d6202c943aSPL ID 01b46020-bf09-4338-9dd9-c0d6202c943aSPL set ID 4f42d132-9a8d-4cd4-ae94-318205fb870eRxCUI 197361, 308135, 308136UNII 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

N464980072509 followed by a unit qualifier and the quantity

Package 64980-0725-09. 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 are 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 tab…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64980-725

What is NDC 64980-725?
64980-725 is the product NDC for Amlodipine Besylate, Amlodipine besylate 10 mg/1 tablet, listed with the FDA by Rising Pharma Holdings, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Amlodipine Besylate.
What is the active ingredient?
Amlodipine besylate.
Who is the labeler?
Rising Pharma Holdings, Inc., NDC labeler code 64980. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amlodipine Besylate?
171 other product NDCs are listed under this name. See all Amlodipine Besylate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Amlodipine Besylate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralAmerican Health Packaging60687-96160687-0961-01
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralAmerican Health Packaging60687-97260687-0972-01
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralDirect_Rx72189-68972189-0689-90
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralCoupler LLC67046-115767046-1157-03
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralRising Pharma Holdings, Inc.64980-72364980-0723-0964980-0723-10
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralRising Pharma Holdings, Inc.64980-72464980-0724-0964980-0724-10
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-01787441-0017-01
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralUnit Dose Solutions, Inc.87441-01687441-0016-01
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralSafecor Health LLC48433-15648433-0156-20
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralSafecor Health LLC48433-15548433-0155-20

All 172 Amlodipine Besylate NDCs

Other NDCs under ANDA 201380

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

FDA NDC Directory listings under ANDA 201380
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralRising Pharma Holdings, Inc.64980-723
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralRising Pharma Holdings, Inc.64980-724

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