What is NDC 43063-548?

43063-548 is the product NDC for Lovastatin, Lovastatin 40 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lovastatin?

71 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lovastatin NDC 43063-548 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43063-548Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43063-0548Add 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
43063-548-14	43063054814	14 TABLET in 1 BOTTLE, PLASTIC (43063-548-14)Marketed from Nov 15, 2014
43063-548-30	43063054830	30 TABLET in 1 BOTTLE, PLASTIC (43063-548-30)Marketed from Nov 15, 2014
43063-548-90	43063054890	90 TABLET in 1 BOTTLE, PLASTIC (43063-548-90)Marketed from Nov 15, 2014
43063-548-93	43063054893	180 TABLET in 1 BOTTLE, PLASTIC (43063-548-93)Marketed from Dec 24, 2014
43063-548-95	43063054895	1000 TABLET in 1 BOTTLE, PLASTIC (43063-548-95)Marketed from Sep 16, 2022

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): Lovastatin
Generic name (nonproprietary): lovastatin
Active ingredients: Lovastatin — 40 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PD-Rx Pharmaceuticals, Inc.NDC labeler code 43063
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075991
Marketing start: Nov 25, 2002
Listing expires: Dec 31, 2026
Other FDA classes: Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers: Product ID 43063-548_2f3a8f82-8530-3a64-e063-6294a90aa0b0SPL ID 2f3a8f82-8530-3a64-e063-6294a90aa0b0SPL set ID eea93a4b-f804-4b9c-aabf-e906f03c1e80RxCUI 197905UNII 9LHU78OQFDUPC 0343063548905
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

N443063054814 followed by a unit qualifier and the quantity

Package 43063-0548-14. 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 28, 2025.

Indications (excerpt from the label)

Indications and Usage Therapy with lovastatin should be a component of multiple risk factor intervention in those individuals with dyslipidemia at risk for atherosclerotic vascular disease. Lovastatin should be used in addition to a diet restricted in saturated fat and cholesterol as part of a treatment strategy to lower total-C and LDL-C to target levels when the response to diet and other nonpharmacological measures alone has been inadequate to reduce risk. Primary Prevention of Coronary Heart Disease In individuals without symptomatic cardiovascular disease, average to moderately elevated total-C and LDL-C, and below average HDL-C, lovastatin is indicated to reduce the risk of: Myocardial…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43063-548

What is NDC 43063-548?: 43063-548 is the product NDC for Lovastatin, Lovastatin 40 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lovastatin.
What is the active ingredient?: Lovastatin.
Who is the labeler?: PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lovastatin?: 71 other product NDCs are listed under this name. See all Lovastatin 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 Lovastatin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lovastatin	Lovastatin 40 mg/1	TabletOral	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	83209-143	83209-0143-30
Lovastatin	Lovastatin 20 mg/1	TabletOral	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	83209-468	83209-0468-30
Lovastatin	Lovastatin 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-873	51655-0873-52
Lovastatin	Lovastatin 20 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-8326	68788-8326-0168788-8326-0368788-8326-06+1 more
Lovastatin	Lovastatin 40 mg/1	TabletOral	Northwind Health Company, LLC	51655-469	51655-0469-2651655-0469-52
Lovastatin	Lovastatin 40 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-8232	68788-8232-03
Lovastatin	Lovastatin 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-3064	70518-3064-0070518-3064-01
Lovastatin	Lovastatin 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-686	51655-0686-52
Lovastatin	Lovastatin 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-558	51655-0558-2651655-0558-52
Lovastatin	Lovastatin 40 mg/1	TabletOral	REMEDYREPACK INC.	70518-2425	70518-2425-01

All 72 Lovastatin NDCs

Other NDCs under ANDA 075991

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

FDA NDC Directory listings under ANDA 075991
Product	Strength	Form · route	Labeler	Product NDC
Lovastatin	Lovastatin 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-692
Lovastatin	Lovastatin 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-939
Lovastatin	Lovastatin 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-983
Lovastatin	Lovastatin 40 mg/1	TabletOral	A-S Medication Solutions	50090-0761
Lovastatin	Lovastatin 20 mg/1	TabletOral	A-S Medication Solutions	50090-3881
Lovastatin	Lovastatin 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-686
Lovastatin	Lovastatin 10 mg/1	TabletOral	Carlsbad Technology, Inc.	61442-141
Lovastatin	Lovastatin 20 mg/1	TabletOral	Carlsbad Technology, Inc.	61442-142
Lovastatin	Lovastatin 40 mg/1	TabletOral	Carlsbad Technology, Inc.	61442-143
Lovastatin	Lovastatin 20 mg/1	TabletOral	Proficient Rx LP	63187-090
Lovastatin	Lovastatin 10 mg/1	TabletOral	Proficient Rx LP	63187-194
Lovastatin	Lovastatin 40 mg/1	TabletOral	Proficient Rx LP	63187-345
Lovastatin	Lovastatin 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-1018
Lovastatin	Lovastatin 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-1178
Lovastatin	Lovastatin 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-1191
Lovastatin	Lovastatin 20 mg/1	TabletOral	Bryant Ranch Prepack	63629-1464
Lovastatin	Lovastatin 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-3583
Lovastatin	Lovastatin 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-506
Lovastatin	Lovastatin 40 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-561
Lovastatin	Lovastatin 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3127

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