NDC codes

FDA NDC Directory
Product NDC (as listed)82009-028Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82009-0028Add 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
82009-028-10820090028101000 TABLET in 1 BOTTLE (82009-028-10)Marketed from Dec 1, 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
Generic name (nonproprietary)
amlodipine besylate
Active ingredients
Amlodipine besylate — 10 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 82009-028_72ad7e01-b3db-46b3-af3f-746e5ec70cd0SPL ID 72ad7e01-b3db-46b3-af3f-746e5ec70cd0SPL set ID c262dedb-1d13-4447-9355-f11e1dbbfb4dRxCUI 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

N482009002810 followed by a unit qualifier and the quantity

Package 82009-0028-10. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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/1TabletOralBryant Ranch Prepack71335-0218
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/1TabletOralREMEDYREPACK INC.70518-0297
Amlodipine BesylateAmlodipine besylate 5 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-027

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