What is NDC 71335-2507?

71335-2507 is the product NDC for Amlodipine Besylate, Amlodipine besylate 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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?

167 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Amlodipine Besylate NDC 71335-2507

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2507Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2507Add 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
71335-2507-0	7133525070071335250700	7 TABLET in 1 BOTTLE (71335-2507-0)Marketed from Oct 7, 2024
71335-2507-1	7133525070171335250701	30 TABLET in 1 BOTTLE (71335-2507-1)Marketed from Oct 7, 2024
71335-2507-2	7133525070271335250702	90 TABLET in 1 BOTTLE (71335-2507-2)Marketed from Oct 7, 2024
71335-2507-3	7133525070371335250703	60 TABLET in 1 BOTTLE (71335-2507-3)Marketed from Oct 7, 2024
71335-2507-4	7133525070471335250704	120 TABLET in 1 BOTTLE (71335-2507-4)Marketed from Oct 7, 2024
71335-2507-5	7133525070571335250705	100 TABLET in 1 BOTTLE (71335-2507-5)Marketed from Oct 7, 2024
71335-2507-6	7133525070671335250706	800 TABLET in 1 BOTTLE (71335-2507-6)Marketed from Oct 7, 2024
71335-2507-7	7133525070771335250707	1000 TABLET in 1 BOTTLE (71335-2507-7)Marketed from Oct 7, 2024
71335-2507-8	7133525070871335250708	180 TABLET in 1 BOTTLE (71335-2507-8)Marketed from Oct 7, 2024
71335-2507-9	7133525070971335250709	10 TABLET in 1 BOTTLE (71335-2507-9)Marketed from Oct 7, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078043
Marketing start: Aug 15, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 71335-2507_97992e54-4553-4e64-97f8-0d04b6ff3133SPL ID 97992e54-4553-4e64-97f8-0d04b6ff3133SPL set ID 49d69d27-2a75-4a07-bfb9-24f8af853138RxCUI 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

N471335250700 followed by a unit qualifier and the quantity

Package 71335-2507-00. 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 Oct 7, 2024.

Indications (excerpt from the label)

Amlodipine besylate tablets are calcium channel blocker and may be used alone or in combination with other antihypertensive and antianginal agents for the treatment of: •Hypertension ( 1.1 ) о 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 ) о Chronic Stable Angina о Vasospastic Angina (Prinzmetal's or Variant Angina) о Angiographically Documented Coronary Artery Disease in patients without heart failure or an ejection fraction < 40% 1.1 Hypertension Amlodipine besylate tablets…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2507

What is NDC 71335-2507?: 71335-2507 is the product NDC for Amlodipine Besylate, Amlodipine besylate 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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?: 167 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	American Health Packaging	60687-961	60687-0961-01
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	American Health Packaging	60687-972	60687-0972-01
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Direct_Rx	72189-689	72189-0689-90
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Coupler LLC	67046-1157	67046-1157-03
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-016	87441-0016-01
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-017	87441-0017-01
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Safecor Health LLC	48433-155	48433-0155-20
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Safecor Health LLC	48433-156	48433-0156-20
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Safecor Health LLC	48433-157	48433-0157-20
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4629	70518-4629-0070518-4629-02

All 168 Amlodipine Besylate NDCs

Other NDCs under ANDA 078043

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

FDA NDC Directory listings under ANDA 078043
Product	Strength	Form · route	Labeler	Product NDC
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	A-S Medication Solutions	50090-5354
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	A-S Medication Solutions	50090-5355
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Coupler LLC	67046-1157
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3698
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-233
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-455
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-721
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4082
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4085
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Proficient Rx LP	82804-164