NDC codes

FDA NDC Directory
Product NDC (as listed)82009-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82009-0001Add 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
82009-001-10820090001101000 TABLET, FILM COATED in 1 BOTTLE (82009-001-10)Marketed from Nov 23, 2021
82009-001-908200900019090 TABLET, FILM COATED in 1 BOTTLE (82009-001-90)Marketed from Nov 23, 2021

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 propylene glycol solvate — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
QuallentNDC labeler code 82009
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090548
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 82009-001_30b5cd59-2e05-be79-38bd-c81f157aa41dSPL ID 30b5cd59-2e05-be79-38bd-c81f157aa41dSPL set ID f00a83aa-3f1d-566d-b9bb-f396f22a27cbRxCUI 259255, 617310, 617311, 617312UNII YRZ789OWMI
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

N482009000110 followed by a unit qualifier and the quantity

Package 82009-0001-10. 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)

About NDC 82009-001

What is NDC 82009-001?
82009-001 is the product NDC for Atorvastatin Calcium, Atorvastatin calcium propylene glycol solvate 10 mg/1 tablet, film coated, listed with the FDA by Quallent. It has 2 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 propylene glycol solvate.
Who is the labeler?
Quallent, NDC labeler code 82009. 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?
385 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 386 Atorvastatin Calcium NDCs

Other NDCs under ANDA 090548

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

FDA NDC Directory listings under ANDA 090548
ProductStrengthForm · routeLabelerProduct NDC
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralAvPAK50268-095
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6291
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6506
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralAvPAK50268-093
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralAvPAK50268-094
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-613
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6480
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6479
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6481
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6482
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6290
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6505
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-453
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3961
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-496
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6292
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralQuallent82009-004
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralQuallent82009-002
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralQuallent82009-003
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6293

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