NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2924Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2924Add 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
71335-2924-17133529240130 TABLET, FILM COATED in 1 BOTTLE (71335-2924-1)Marketed from Oct 30, 2025

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 and Atorvastatin
Generic name (nonproprietary)
amlodipine and atorvastatin
Active ingredients
Amlodipine besylate — 10 mg/1Atorvastatin calcium trihydrate — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205199
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2924_935246fc-48db-4814-a8ae-e307b9b1f7b2SPL ID 935246fc-48db-4814-a8ae-e307b9b1f7b2SPL set ID be709711-e7ee-403f-ad43-873761deee37RxCUI 597987UNII 864V2Q084H, 48A5M73Z4Q
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; HMG-CoA Reductase Inhibitor

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

N471335292401 followed by a unit qualifier and the quantity

Package 71335-2924-01. 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 and atorvastatin tablets are indicated in patients for whom treatment with both amlodipine and atorvastatin is appropriate. Amlodipine Hypertension Amlodipine is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including amlodipine. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 205199

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

FDA NDC Directory listings under ANDA 205199
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralApotex Corp.60505-3478
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralApotex Corp.60505-3488
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralApotex Corp.60505-3479
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralApotex Corp.60505-3483
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralApotex Corp.60505-3484
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralApotex Corp.60505-3493
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralApotex Corp.60505-3489
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralApotex Corp.60505-3492
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2092
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2090
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2091
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2093
Amlodipine and AtorvastatinAmlodipine besylate 5 mg/1; Atorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2094
Amlodipine and AtorvastatinAmlodipine besylate 10 mg/1; Atorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-3076

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in