What is NDC 72189-059?

72189-059 is the product NDC for Pravastatin Sodium, Pravastatin sodium 10 mg/1 tablet, listed with the FDA by DIRECT RX. It has 1 package NDC, shown above in 10- and 11-digit form.

DIRECT RX, NDC labeler code 72189. 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 72189-059 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-059Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0059Add 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	Copy
72189-059-90	7218900599072189005990	90 TABLET in 1 BOTTLE (72189-059-90)Marketed from Nov 11, 2019

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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: DIRECT RXNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076341
Marketing start: Nov 11, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 72189-059_2be8f6ba-328a-86ab-e063-6394a90acb89SPL ID 2be8f6ba-328a-86ab-e063-6394a90acb89SPL set ID 97178675-3691-2d93-e053-2995a90aa5c1RxCUI 904458, 904467, 904475, 904481UNII 3M8608UQ61
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

N472189005990 followed by a unit qualifier and the quantity

Package 72189-0059-90. 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 Jan 17, 2025.

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. 1.1 Prevention of Cardiovascular Disease In hypercholesterolemic patients without clinically evident coronary heart disease (CHD), pravastatin sodium tablets are indicated to: reduce the risk of myocardial infarction (MI). reduce the risk of undergoing myocardial revascularization procedures. reduce th…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-059

What is NDC 72189-059?: 72189-059 is the product NDC for Pravastatin Sodium, Pravastatin sodium 10 mg/1 tablet, listed with the FDA by DIRECT RX. It has 1 package NDC, 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?: DIRECT RX, NDC labeler code 72189. 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	Quallent	82009-007
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Apotex Corp.	60505-1323
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Quallent	82009-006
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Major Pharmaceuticals	0904-5892
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Quallent	82009-008
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Bryant Ranch Prepack	71335-0692
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Bryant Ranch Prepack	71335-2253
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Major Pharmaceuticals	0904-5893
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-7275
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	Proficient Rx LP	71205-516
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-8833
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-143
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Northwind Health Company, LLC	51655-976
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Bryant Ranch Prepack	63629-8835
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-1938
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Bryant Ranch Prepack	63629-8836
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-161
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0549

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