What is NDC 84386-032?

84386-032 is the product NDC for Pravastatin sodium, Pravastatin sodium 20 mg/1 tablet, listed with the FDA by Aurobindo Pharma Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.

Aurobindo Pharma Limited, NDC labeler code 84386. 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 84386-032 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)84386-032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84386-0032Add 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
84386-032-90	8438600329084386003290	90 TABLET in 1 BOTTLE (84386-032-90)Marketed from Feb 27, 2025
84386-032-99	8438600329984386003299	1000 TABLET in 1 BOTTLE (84386-032-99)Marketed from Feb 27, 2025

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 — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Aurobindo Pharma LimitedNDC labeler code 84386
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076056
Marketing start: Feb 27, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 84386-032_cf6f7031-33b9-40d3-bc87-32f1b6af98f2SPL ID cf6f7031-33b9-40d3-bc87-32f1b6af98f2SPL set ID cf6f7031-33b9-40d3-bc87-32f1b6af98f2RxCUI 904458, 904467, 904475UNII 3M8608UQ61UPC 0384386032900, 0384386031903, 0384386033907
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

N484386003290 followed by a unit qualifier and the quantity

Package 84386-0032-90. 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 Feb 18, 2025.

Indications (excerpt from the label)

Pravastatin sodium tablets are indicated: To reduce the risk of myocardial infarction, myocardial revascularization procedures, and cardiovascular mortality in adults with elevated low-density lipoprotein cholesterol (LDL-C) without clinically evident coronary heart disease (CHD). To reduce the risk of coronary death, myocardial infarction, myocardial revascularization procedures, stroke or transient ischemic attack, and slow the progression of coronary atherosclerosis in adults with clinically evident CHD. As an adjunct to diet to reduce LDL-C in adults with primary hyperlipidemia. As an adjunct to diet to reduce LDL-C in pediatric patients ages 8 years and older with heterozygous familial …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 84386-032

What is NDC 84386-032?: 84386-032 is the product NDC for Pravastatin sodium, Pravastatin sodium 20 mg/1 tablet, listed with the FDA by Aurobindo Pharma Limited. It has 2 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?: Aurobindo Pharma Limited, NDC labeler code 84386. 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 30 mg/1	TabletOral	Havix Group Inc d-b-a Aavis Pharmaceuticals	71337-289	71337-0289-09
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 80 mg/1	TabletOral	Aurobindo Pharma Limited	84386-167	84386-0167-9084386-0167-99
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 40 mg/1	TabletOral	Amici Pharma, Inc.	69292-103	69292-0103-1069292-0103-5069292-0103-90
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 076056

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

FDA NDC Directory listings under ANDA 076056
Product	Strength	Form · route	Labeler	Product NDC
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-7947
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-7948
Pravastatin sodium	Pravastatin sodium 10 mg/1	TabletOral	Aurobindo Pharma Limited	84386-031
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Aurobindo Pharma Limited	84386-033
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-0973
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3895
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Proficient Rx LP	71205-294
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8871
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	A-S Medication Solutions	50090-6898
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4049
Pravastatin sodium	Pravastatin sodium 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4059
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-4339
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	Safecor Health LLC	48433-148
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Safecor Health LLC	48433-149
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-4206
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	A-S Medication Solutions	50090-8161
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-7201
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3788
Pravastatin sodium	Pravastatin sodium 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4408
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Northwind Health Company, LLC	82868-096