What is NDC 70518-0297?

70518-0297 is the product NDC for Amlodipine Besylate, Amlodipine besylate 10 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-0297

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-0297Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-0297Add 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
70518-0297-0	7051802970070518029700	30 TABLET in 1 BLISTER PACK (70518-0297-0)Marketed from Mar 8, 2017
70518-0297-1	7051802970170518029701	90 TABLET in 1 BOTTLE, PLASTIC (70518-0297-1)Marketed from Apr 24, 2017
70518-0297-4	7051802970470518029704	50 POUCH in 1 BOX (70518-0297-4) / 1 TABLET in 1 POUCH (70518-0297-5)Marketed from Apr 22, 2026

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: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077073
Marketing start: Mar 8, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers: Product ID 70518-0297_55049337-b779-4bb3-e063-6394a90a7e99SPL ID 55049337-b779-4bb3-e063-6394a90a7e99SPL set ID a6fa364c-3ad6-4bf9-b9ee-5ec3b1a7eb55RxCUI 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

N470518029700 followed by a unit qualifier and the quantity

Package 70518-0297-00. 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 Jun 24, 2026.

Indications (excerpt from the label)

Amlodipine besylate tablet, USP 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) o 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) o Chronic Stable Angina o Vasospastic Angina (Prinzmetal's or Variant Angina) o Angiographically Documented Coronary Artery Disease in patients without heart failure or an ejection fraction < 40% 1.1 Hypertension Amlodipine besylate tabl…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-0297

What is NDC 70518-0297?: 70518-0297 is the product NDC for Amlodipine Besylate, Amlodipine besylate 10 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 3 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 077073

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

FDA NDC Directory listings under ANDA 077073
Product	Strength	Form · route	Labeler	Product NDC
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-764
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Northwind Health Company, LLC	51655-044
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-869
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Proficient Rx LP	63187-914
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Redpharm Drug	67296-2297
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-1980
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8627
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Cipla USA Inc.	69097-126
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Cipla USA Inc.	69097-127
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Cipla USA Inc.	69097-128
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-0835
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-0218
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0473
Amlodipine Besylate	Amlodipine besylate 2.5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-026
Amlodipine Besylate	Amlodipine besylate 5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-027
Amlodipine Besylate	Amlodipine besylate 10 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-028