What is NDC 68071-2967?

68071-2967 is the product NDC for Atorvastatin calcium, Atorvastatin 20 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?

389 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Atorvastatin calcium NDC 68071-2967

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2967Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2967Add 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 NDC	11-digit (billing)	Package
68071-2967-3	6807129670368071296703	30 TABLET in 1 BOTTLE (68071-2967-3)Marketed from Mar 27, 2023
68071-2967-6	6807129670668071296706	60 TABLET in 1 BOTTLE (68071-2967-6)Marketed from Mar 27, 2023
68071-2967-9	6807129670968071296709	90 TABLET in 1 BOTTLE (68071-2967-9)Marketed from Mar 27, 2023

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 — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213853
Marketing start: Aug 26, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 68071-2967_10abb3fc-2512-255d-e063-6394a90ae0deSPL ID 10abb3fc-2512-255d-e063-6394a90ae0deSPL set ID f7e8c8d2-b74e-6afd-e053-6394a90af83eRxCUI 617310UNII A0JWA85V8FUPC 0368071296792
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

N468071296703 followed by a unit qualifier and the quantity

Package 68071-2967-03. 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 Feb 5, 2024.

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 68071-2967

What is NDC 68071-2967?: 68071-2967 is the product NDC for Atorvastatin calcium, Atorvastatin 20 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 3 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.
Who is the labeler?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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?: 389 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Atorvastatin calcium	Atorvastatin calcium trihydrate 40 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-979	60760-0979-30
Atorvastatin Calcium	Atorvastatin calcium trihydrate 80 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0284	55154-0284-06
Atorvastatin Calcium	Atorvastatin calcium trihydrate 10 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-681	72189-0681-30
Atorvastatin Calcium	Atorvastatin calcium trihydrate 10 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals, Inc.	0480-3585	00480-3585-1000480-3585-98
Atorvastatin Calcium	Atorvastatin calcium propylene glycol solvate 40 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-013	87441-0013-01
Atorvastatin Calcium	Atorvastatin calcium trihydrate 20 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals, Inc.	0480-3586	00480-3586-1000480-3586-98
Atorvastatin Calcium	Atorvastatin calcium trihydrate 40 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals, Inc.	0480-3587	00480-3587-1000480-3587-98
Atorvastatin Calcium	Atorvastatin calcium trihydrate 10 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1677	67046-1677-03
Atorvastatin Calcium	Atorvastatin calcium trihydrate 80 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals, Inc.	0480-3588	00480-3588-1000480-3588-98
Atorvastatin Calcium	Atorvastatin calcium trihydrate 80 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1666	67046-1666-03

All 390 Atorvastatin calcium NDCs

Other NDCs under ANDA 213853

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

FDA NDC Directory listings under ANDA 213853
Product	Strength	Form · route	Labeler	Product NDC
Atorvastatin calcium	Atorvastatin 10 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-039
Atorvastatin calcium	Atorvastatin 20 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-040
Atorvastatin calcium	Atorvastatin 40 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-041
Atorvastatin calcium	Atorvastatin 80 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-042
Atorvastatin calcium	Atorvastatin 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-3783
Atorvastatin calcium	Atorvastatin 80 mg/1	TabletOral	REMEDYREPACK INC.	70518-3848
Atorvastatin calcium	Atorvastatin 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4321
Atorvastatin calcium	Atorvastatin 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-2213
Atorvastatin calcium	Atorvastatin 40 mg/1	TabletOral	Bryant Ranch Prepack	71335-2697
Atorvastatin calcium	Atorvastatin 80 mg/1	TabletOral	Bryant Ranch Prepack	71335-9646
Atorvastatin Calcium	Atorvastatin 20 mg/1	TabletOral	DirectRX	72189-291
Atorvastatin Calcium	Atorvastatin 10 mg/1	TabletOral	Direct_Rx	72189-531
Atorvastatin calcium	Atorvastatin 10 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-255
Atorvastatin calcium	Atorvastatin 20 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-256
Atorvastatin calcium	Atorvastatin 40 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-257
Atorvastatin calcium	Atorvastatin 80 mg/1	TabletOral	NIVAGEN PHARMACEUTICALS, INC.	75834-258
Atorvastatin calcium	Atorvastatin 40 mg/1	TabletOral	Proficient Rx LP	82804-056