What is NDC 71337-290?

71337-290 is the product NDC for Pravastatin Sodium, Pravastatin sodium 60 mg/1 tablet, listed with the FDA by Havix Group Inc d-b-a Aavis Pharmaceuticals. It has 1 package NDC, shown above in 10- and 11-digit form.

Havix Group Inc d-b-a Aavis Pharmaceuticals, NDC labeler code 71337. 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 71337-290 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71337-290Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71337-0290Add 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
71337-290-09	7133702900971337029009	90 TABLET in 1 BOTTLE (71337-290-09)Marketed from Nov 5, 2026

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 — 60 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Havix Group Inc d-b-a Aavis PharmaceuticalsNDC labeler code 71337
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077491
Marketing start: Nov 5, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 71337-290_bfc0f449-8b64-4f07-b6b7-961f8cc3b9bbSPL ID bfc0f449-8b64-4f07-b6b7-961f8cc3b9bbSPL set ID 222b90fd-f070-4fa8-8f8b-720133cb2b0aUNII 3M8608UQ61UPC 0371337290090
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

N471337029009 followed by a unit qualifier and the quantity

Package 71337-0290-09. 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 Nov 6, 2026.

Full label on DailyMed (opens in a new tab)

About NDC 71337-290

What is NDC 71337-290?: 71337-290 is the product NDC for Pravastatin Sodium, Pravastatin sodium 60 mg/1 tablet, listed with the FDA by Havix Group Inc d-b-a Aavis Pharmaceuticals. 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?: Havix Group Inc d-b-a Aavis Pharmaceuticals, NDC labeler code 71337. 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 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
Pravastatin sodium	Pravastatin sodium 40 mg/1	TabletOral	Northwind Health Company, LLC	82868-096	82868-0096-30

All 185 Pravastatin Sodium NDCs

Other NDCs under ANDA 077491

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

FDA NDC Directory listings under ANDA 077491
Product	Strength	Form · route	Labeler	Product NDC
Pravastatin Sodium	Pravastatin sodium 10 mg/1	TabletOral	Amici Pharma, Inc.	69292-101
Pravastatin Sodium	Pravastatin sodium 20 mg/1	TabletOral	Amici Pharma, Inc.	69292-102
Pravastatin Sodium	Pravastatin sodium 40 mg/1	TabletOral	Amici Pharma, Inc.	69292-103
Pravastatin Sodium	Pravastatin sodium 80 mg/1	TabletOral	Amici Pharma, Inc.	69292-104