NDC codes

FDA NDC Directory
Product NDC (as listed)71335-3179Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-3179Add 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
71335-3179-17133531790130 TABLET, FILM COATED in 1 BOTTLE (71335-3179-1)Marketed from Sep 8, 2026
71335-3179-27133531790260 TABLET, FILM COATED in 1 BOTTLE (71335-3179-2)Marketed from Sep 8, 2026
71335-3179-37133531790390 TABLET, FILM COATED in 1 BOTTLE (71335-3179-3)Marketed from Sep 8, 2026
71335-3179-471335317904180 TABLET, FILM COATED in 1 BOTTLE (71335-3179-4)Marketed from Sep 8, 2026

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 — 80 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217118
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71335-3179_4c68ba68-378b-4e23-b8da-9af11d4963a2SPL ID 4c68ba68-378b-4e23-b8da-9af11d4963a2
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

N471335317901 followed by a unit qualifier and the quantity

Package 71335-3179-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 217118

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

FDA NDC Directory listings under ANDA 217118
ProductStrengthForm · routeLabelerProduct NDC
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralCoupler LLC67046-1666
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralCoupler LLC67046-1677
Atorvastatin CalciumAtorvastatin calcium trihydrate 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-608
Atorvastatin CalciumAtorvastatin calcium trihydrate 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-606
Atorvastatin CalciumAtorvastatin calcium trihydrate 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-607
Atorvastatin CalciumAtorvastatin calcium trihydrate 80 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-609

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