AMLODIPINE BESYLATE 10 mg (amlodipine besylate) NDC 72789-262

NDC codes

FDA NDC Directory

Product NDC (as listed)72789-262Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72789-0262Add 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
72789-262-30	72789026230	30 TABLET in 1 BOTTLE, PLASTIC (72789-262-30)Marketed from Apr 21, 2023
72789-262-60	72789026260	60 TABLET in 1 BOTTLE, PLASTIC (72789-262-60)Marketed from Apr 21, 2023
72789-262-90	72789026290	90 TABLET in 1 BOTTLE, PLASTIC (72789-262-90)Marketed from Jul 15, 2022
72789-262-95	72789026295	1000 TABLET in 1 BOTTLE, PLASTIC (72789-262-95)Marketed from Jul 15, 2022

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 10 mgSuffix: 10 mg
Generic name (nonproprietary): amlodipine besylate
Active ingredients: Amlodipine besylate — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PD-Rx Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078414
Marketing start: Oct 1, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 72789-262_56d162c9-8f01-cab0-e063-6294a90ab853SPL ID 56d162c9-8f01-cab0-e063-6294a90ab853SPL set ID 1080fcea-a5da-499d-a855-690c13559071RxCUI 197361, 308135, 308136UNII 864V2Q084HUPC 0372789262956, 0372789261959, 0372789260952
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

N472789026230 followed by a unit qualifier and the quantity

Package 72789-0262-30. 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 Jul 17, 2026.

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 tablets are in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078414

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

FDA NDC Directory listings under ANDA 078414
Product	Strength	Form · route	Labeler	Product NDC
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	Proficient Rx LP	82804-971
AMLODIPINE BESYLATE 2.5 mgamlodipine besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-802
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-023
AMLODIPINE BESYLATE 2.5 mgamlodipine besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-021
AMLODIPINE BESYLATE 5 mgamlodipine besylate	Amlodipine besylate 5 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-022
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-830
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3453
AMLODIPINE BESYLATE 5 mgamlodipine besylate	Amlodipine besylate 5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-687
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-978
AMLODIPINE BESYLATE 5 mgamlodipine besylate	Amlodipine besylate 5 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-985
AMLODIPINE BESYLATE 10 mgamlodipine besylate	Amlodipine besylate 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8451
AMLODIPINE BESYLATE 2.5 mgamlodipine besylate	Amlodipine besylate 2.5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-260
AMLODIPINE BESYLATE 5 mgamlodipine besylate	Amlodipine besylate 5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-261
AMLODIPINE BESYLATE 5 mgamlodipine besylate	Amlodipine besylate 5 mg/1	TabletOral	Proficient Rx LP	82804-970
AMLODIPINE BESYLATE 2.5 mgamlodipine besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Proficient Rx LP	82804-969