NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0218Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0218Add 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
71335-0218-0713350218007 TABLET in 1 BOTTLE (71335-0218-0)Marketed from Sep 23, 2022
71335-0218-17133502180130 TABLET in 1 BOTTLE (71335-0218-1)Marketed from Mar 30, 2018
71335-0218-27133502180290 TABLET in 1 BOTTLE (71335-0218-2)Marketed from Feb 26, 2018
71335-0218-37133502180360 TABLET in 1 BOTTLE (71335-0218-3)Marketed from Mar 30, 2018
71335-0218-471335021804120 TABLET in 1 BOTTLE (71335-0218-4)Marketed from Sep 23, 2022
71335-0218-571335021805100 TABLET in 1 BOTTLE (71335-0218-5)Marketed from Sep 23, 2022
71335-0218-671335021806800 TABLET in 1 BOTTLE (71335-0218-6)Marketed from Sep 23, 2022
71335-0218-7713350218071000 TABLET in 1 BOTTLE (71335-0218-7)Marketed from Sep 23, 2022
71335-0218-871335021808180 TABLET in 1 BOTTLE (71335-0218-8)Marketed from Sep 23, 2022
71335-0218-97133502180910 TABLET in 1 BOTTLE (71335-0218-9)Marketed from Sep 23, 2022

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 besylate10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077073
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 71335-0218_9f46a706-45ec-400f-9a85-eacceab1ed05SPL ID 9f46a706-45ec-400f-9a85-eacceab1ed05SPL set ID 215e0890-0484-45e8-a731-aea53821ad8eRxCUI 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

N471335021800 followed by a unit qualifier and the quantity

Package 71335-0218-00. 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 .

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)

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
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-1980
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralNorthwind Health Company, LLC51655-044
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralBryant Ranch Prepack71335-0473
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8627
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralREMEDYREPACK INC.70518-0835
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralRedpharm Drug67296-2297
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralCipla USA Inc.69097-128
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralCipla USA Inc.69097-126
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralCipla USA Inc.69097-127
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralProficient Rx LP63187-914
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralNorthwind Health Company, LLC51655-869
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-764
Amlodipine BesylateAmlodipine besylate 2.5 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-026
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-028
Amlodipine BesylateAmlodipine besylate 10 mg/1TabletOralREMEDYREPACK INC.70518-0297
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-027

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