What is NDC 71205-516?

71205-516 is the product NDC for Pravastatin Sodium, Pravastatin sodium 40 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pravastatin Sodium?

184 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pravastatin Sodium NDC 71205-516 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-516Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0516Add 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
71205-516-30	7120505163071205051630	30 TABLET in 1 BOTTLE (71205-516-30)Marketed from Dec 24, 2020
71205-516-60	7120505166071205051660	60 TABLET in 1 BOTTLE (71205-516-60)Marketed from Dec 24, 2020
71205-516-90	7120505169071205051690	90 TABLET in 1 BOTTLE (71205-516-90)Marketed from Dec 24, 2020

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): Pravastatin Sodium
Generic name (nonproprietary): pravastatin sodium
Active ingredients: Pravastatin sodium — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076341
Marketing start: Jul 18, 2011
Listing expires: Dec 31, 2027
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 71205-516_d1c530da-d15b-4ffc-b2b4-cd1e4dd5e8eeSPL ID d1c530da-d15b-4ffc-b2b4-cd1e4dd5e8eeSPL set ID 2bdfb0ef-2455-4ca2-a117-ce8e26bb2dbcRxCUI 904475UNII 3M8608UQ61UPC 0371205516307
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

N471205051630 followed by a unit qualifier and the quantity

Package 71205-0516-30. 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 Mar 1, 2022.

Indications (excerpt from the label)

Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is indicated as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other nonpharmacologic measures alone has been inadequate. Pravastatin sodium is an HMG-CoA reductase inhibitor (statin) indicated as an adjunctive therapy to diet to: 7. Reduce the risk of MI, revascularization, and cardiovascular mortality in hypercholesterolemic patients without clinically evident CHD. ( 1.1 ) 8. Reduce the risk of total mortality by reduci…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-516

What is NDC 71205-516?: 71205-516 is the product NDC for Pravastatin Sodium, Pravastatin sodium 40 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pravastatin Sodium.
What is the active ingredient?: Pravastatin sodium.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pravastatin Sodium?: 184 other product NDCs are listed under this name. See all Pravastatin Sodium 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 Pravastatin Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pravastatin Sodium	Pravastatin sodium 60 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-290	71337-0290-09
Pravastatin Sodium	Pravastatin sodium 30 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-289	71337-0289-09
Pravastatin sodium	Pravastatin sodium 80 mg/1	TabletOral	Aurobindo Pharma Limited	84386-167	84386-0167-9084386-0167-99
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Amici Pharma, Inc.	69292-103	69292-0103-1069292-0103-5069292-0103-90
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Amici Pharma, Inc.	69292-101	69292-0101-1069292-0101-5069292-0101-90
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Amici Pharma, Inc.	69292-102	69292-0102-1069292-0102-5069292-0102-90
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Amici Pharma, Inc.	69292-104	69292-0104-1069292-0104-5069292-0104-90
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Northwind Health Company, LLC	82868-104	82868-0104-30
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	Safecor Health LLC	48433-148	48433-0148-20
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Safecor Health LLC	48433-149	48433-0149-20

All 185 Pravastatin Sodium NDCs

Other NDCs under ANDA 076341

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

FDA NDC Directory listings under ANDA 076341
Product	Strength	Form · route	Labeler	Product NDC
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8620
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7275
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-143
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8621
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Bryant Ranch Prepack	63629-8835
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1243
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Quallent	82009-006
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Quallent	82009-007
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-8833
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Quallent	82009-008
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Bryant Ranch Prepack	63629-8836
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-1938
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-2024
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-2025
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-161
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Northwind Health Company, LLC	51655-976
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0549
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7009
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7998
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-6826

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