NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2591Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2591Add 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
71335-2591-17133525910130 TABLET in 1 BOTTLE (71335-2591-1)Marketed from Jun 4, 2025
71335-2591-271335259102100 TABLET in 1 BOTTLE (71335-2591-2)Marketed from Jun 4, 2025
71335-2591-37133525910390 TABLET in 1 BOTTLE (71335-2591-3)Marketed from Jun 4, 2025
71335-2591-47133525910460 TABLET in 1 BOTTLE (71335-2591-4)Marketed from Jun 4, 2025
71335-2591-571335259105180 TABLET in 1 BOTTLE (71335-2591-5)Marketed from Jun 4, 2025
71335-2591-67133525910610 TABLET in 1 BOTTLE (71335-2591-6)Marketed from Jun 4, 2025
71335-2591-7713352591077 TABLET in 1 BOTTLE (71335-2591-7)Marketed from Jun 4, 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)
Atorvastatin Calcium
Generic name (nonproprietary)
atorvastatin calcium, film coated
Active ingredients
Atorvastatin calcium trihydrate — 40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209912
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71335-2591_11e721da-80b6-4730-ad52-ad11ec164696SPL ID 11e721da-80b6-4730-ad52-ad11ec164696SPL set ID 9c58c4cd-fe1c-4db7-832c-874766e4da21RxCUI 617311UNII 48A5M73Z4Q
Pharmacologic class
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

N471335259101 followed by a unit qualifier and the quantity

Package 71335-2591-01. 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)

Atorvastatin calcium tablets are indicated: • To reduce the risk of: ○ Myocardial infarction (MI), stroke, revascularization procedures, and angina in adults with multiple risk factors for coronary heart disease (CHD) but without clinically evident CHD ○ MI and stroke in adults with type 2 diabetes mellitus with multiple risk factors for CHD but without clinically evident CHD ○ Non-fatal MI, fatal and non-fatal stroke, revascularization procedures, hospitalization for congestive heart failure, and angina in adults with clinically evident CHD • As an adjunct to diet to reduce low-density lipoprotein cholesterol (LDL-C) in: ○ Adults with primary hyperlipidemia. ○ Adults and pediatric patients …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209912

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

FDA NDC Directory listings under ANDA 209912
ProductStrengthForm · routeLabelerProduct NDC
atorvastatin calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3546
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 80 mg/1TabletOralBryant Ranch Prepack71335-2582
atorvastatin calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 40 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2994
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3868
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 40 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3882
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralBryant Ranch Prepack71335-2388
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3891
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralRising Pharma Holdings, Inc.16571-136
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 20 mg/1TabletOralBryant Ranch Prepack71335-2404
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 80 mg/1TabletOralRising Pharma Holdings, Inc.16571-139
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 20 mg/1TabletOralRising Pharma Holdings, Inc.16571-137
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 40 mg/1TabletOralRising Pharma Holdings, Inc.16571-138
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3912
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8842
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 40 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8887
Atorvastatin Calciumatorvastatin calcium, film coatedAtorvastatin calcium trihydrate 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8693

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