NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1507Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1507Add 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
71335-1507-17133515070130 TABLET, FILM COATED in 1 BOTTLE (71335-1507-1)Marketed from Feb 10, 2020
71335-1507-27133515070260 TABLET, FILM COATED in 1 BOTTLE (71335-1507-2)Marketed from Mar 16, 2020
71335-1507-37133515070390 TABLET, FILM COATED in 1 BOTTLE (71335-1507-3)Marketed from Feb 25, 2020
71335-1507-4713351507049 TABLET, FILM COATED in 1 BOTTLE (71335-1507-4)Marketed from Oct 31, 2024
71335-1507-57133515070528 TABLET, FILM COATED in 1 BOTTLE (71335-1507-5)Marketed from Oct 31, 2024
71335-1507-67133515070620 TABLET, FILM COATED in 1 BOTTLE (71335-1507-6)Marketed from Oct 31, 2024
71335-1507-771335150707180 TABLET, FILM COATED in 1 BOTTLE (71335-1507-7)Marketed from Oct 31, 2024
71335-1507-871335150708100 TABLET, FILM COATED in 1 BOTTLE (71335-1507-8)Marketed from Oct 31, 2024
71335-1507-9713351507097 TABLET, FILM COATED in 1 BOTTLE (71335-1507-9)Marketed from Oct 31, 2024

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
Active ingredients
Atorvastatin calcium trihydrate — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207687
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71335-1507_7fff292f-dba8-4613-a8d0-19ea6cd0e6a8SPL ID 7fff292f-dba8-4613-a8d0-19ea6cd0e6a8SPL set ID cbeb2aa0-24a2-430f-b456-34a4e63e1817RxCUI 617310UNII 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

N471335150701 followed by a unit qualifier and the quantity

Package 71335-1507-01. 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 is 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 a…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1507

What is NDC 71335-1507?
71335-1507 is the product NDC for Atorvastatin Calcium, Atorvastatin calcium trihydrate 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 9 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Atorvastatin Calcium.
What is the active ingredient?
Atorvastatin calcium trihydrate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Atorvastatin Calcium?
383 other product NDCs are listed under this name. See all Atorvastatin Calcium NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Atorvastatin Calcium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-028455154-0284-06
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralDirect_Rx72189-68172189-0681-30
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-358500480-3585-1000480-3585-98
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralUnit Dose Solutions, Inc.87441-01387441-0013-01
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-358600480-3586-1000480-3586-98
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-358700480-3587-1000480-3587-98
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralCoupler LLC67046-167767046-1677-03
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralTeva Pharmaceuticals, Inc.0480-358800480-3588-1000480-3588-98
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralCoupler LLC67046-166667046-1666-03
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1TabletOralREMEDYREPACK INC.70518-459270518-4592-00

All 384 Atorvastatin Calcium NDCs

Other NDCs under ANDA 207687

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

FDA NDC Directory listings under ANDA 207687
ProductStrengthForm · routeLabelerProduct NDC
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-044
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-045
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-046
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-047
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-946
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2389
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5168
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5194
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5198
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-246
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralProficient Rx LP71205-247
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralProficient Rx LP71205-731
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1126
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1388

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