NDC codes

FDA NDC Directory
Product NDC (as listed)50268-094Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50268-0094Add 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
50268-094-155026800941550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-094-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-094-11)Marketed from Jun 28, 2016

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 — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
AvPAKNDC labeler code 50268
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 50268-094_4dc870e1-0b0c-9b87-e063-6294a90a1845SPL ID 4dc870e1-0b0c-9b87-e063-6294a90a1845SPL set ID b687ba81-cb24-bbdf-5dd9-ab0e53dd480bRxCUI 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

N450268009415 followed by a unit qualifier and the quantity

Package 50268-0094-15. 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: 1. Myocardial infarction (MI), stroke, revascularization procedures, and angina in adults with multiple risk factors for coronary heart disease (CHD) but without clinically evident CHD 2.MI and stroke in adults with type 2 diabetes mellitus with multiple risk factors for CHD but without clinically evident CHD 3. 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: 1. Adults with primary hyperlipidemia. 2. Adults and pediatric patients …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50268-094

What is NDC 50268-094?
50268-094 is the product NDC for Atorvastatin Calcium, Atorvastatin calcium propylene glycol solvate 20 mg/1 tablet, film coated, listed with the FDA by AvPAK. It has 1 package NDC, 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?
AvPAK, NDC labeler code 50268. 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 10 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-5884
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6293
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralQPharma, Inc.42708-014
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralQPharma, Inc.42708-013
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-6646
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralProficient Rx LP63187-108
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralProficient Rx LP63187-109
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0186
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-881
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3813
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralQPharma, Inc.42708-108
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-2765
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0224
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 80 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7289
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-920
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7628
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7630
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-1712
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 40 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-099
Atorvastatin CalciumAtorvastatin calcium propylene glycol solvate 10 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-097

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