NDC codes

FDA NDC Directory
Product NDC (as listed)71610-744Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0744Add 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
71610-744-157161007441515 TABLET, FILM COATED in 1 BOTTLE (71610-744-15)Marketed from Oct 24, 2023
71610-744-307161007443030 TABLET, FILM COATED in 1 BOTTLE (71610-744-30)Marketed from Oct 24, 2023
71610-744-457161007444545 TABLET, FILM COATED in 1 BOTTLE (71610-744-45)Marketed from Oct 24, 2023
71610-744-537161007445360 TABLET, FILM COATED in 1 BOTTLE (71610-744-53)Marketed from Oct 24, 2023
71610-744-607161007446090 TABLET, FILM COATED in 1 BOTTLE (71610-744-60)Marketed from Oct 24, 2023
71610-744-7071610074470120 TABLET, FILM COATED in 1 BOTTLE (71610-744-70)Marketed from Oct 24, 2023

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)
Atorvastatin Calcium
Generic name (nonproprietary)
atorvastatin calcium
Active ingredients
Atorvastatin calcium trihydrate20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205519
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71610-744_5866cff8-7c35-4050-a75f-5e235b9d39b2SPL ID 5866cff8-7c35-4050-a75f-5e235b9d39b2SPL set ID 3dbeae00-89ab-48a6-9e57-8048facb2294RxCUI 259255, 617310, 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

N471610074415 followed by a unit qualifier and the quantity

Package 71610-0744-15. 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 aged 10 years

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 205519

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

FDA NDC Directory listings under ANDA 205519
ProductStrengthForm · routeLabelerProduct NDC
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8469
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8470
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8471
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8472
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralRadha Pharmaceuticals, Inc.77771-454
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralRadha Pharmaceuticals, Inc.77771-451
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralRadha Pharmaceuticals, Inc.77771-452
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralRadha Pharmaceuticals, Inc.77771-453
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-036
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2238
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3267
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-163
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralCipla USA Inc.,69097-899
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralCipla USA Inc.,69097-897
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralCipla USA Inc.,69097-898
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1555
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralCipla USA Inc.,69097-911
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1554
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1556
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-452

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