NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9642Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9642Add 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 NDC11-digit (billing)PackageCopy
71335-9642-1713359642017133596420130 TABLET, FILM COATED in 1 BOTTLE (71335-9642-1)Marketed from Feb 27, 2023
71335-9642-2713359642027133596420260 TABLET, FILM COATED in 1 BOTTLE (71335-9642-2)Marketed from Feb 27, 2023
71335-9642-37133596420371335964203100 TABLET, FILM COATED in 1 BOTTLE (71335-9642-3)Marketed from Mar 3, 2025
71335-9642-4713359642047133596420490 TABLET, FILM COATED in 1 BOTTLE (71335-9642-4)Marketed from Feb 17, 2023
71335-9642-57133596420571335964205120 TABLET, FILM COATED in 1 BOTTLE (71335-9642-5)Marketed from Mar 12, 2025
71335-9642-67133596420671335964206180 TABLET, FILM COATED in 1 BOTTLE (71335-9642-6)Marketed from Apr 15, 2026
71335-9642-771335964207713359642073 TABLET, FILM COATED in 1 BOTTLE (71335-9642-7)Marketed from Apr 15, 2026
71335-9642-8713359642087133596420810 TABLET, FILM COATED in 1 BOTTLE (71335-9642-8)Marketed from Apr 15, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Simvastatin
Generic name (nonproprietary)
simvastatin
Active ingredients
Simvastatin — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078103
Marketing start
Listing expires
Other FDA classes
Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
Identifiers
Product ID 71335-9642_16a69c73-1437-4b33-b8d6-b549e1040ce5SPL ID 16a69c73-1437-4b33-b8d6-b549e1040ce5SPL set ID 5c760852-800b-463e-8059-06a9a82c2225RxCUI 312961UNII AGG2FN16EV
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

N471335964201 followed by a unit qualifier and the quantity

Package 71335-9642-01. 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 .

Indications (excerpt from the label)

Simvastatin tablets USP are indicated: To reduce the risk of total mortality by reducing risk of coronary heart disease death, non-fatal myocardial infarction and stroke, and the need for coronary and non-coronary revascularization procedures in adults with established coronary heart disease, cerebrovascular disease, peripheral vascular disease, and/or diabetes, who are at high risk of coronary heart disease events. As an adjunct to diet to reduce low-density lipoprotein cholesterol (LDL-C): In adults with primary hyperlipidemia. In adults and pediatric patients aged 10 years and older with heterozygous familial hypercholesterolemia (HeFH). As an adjunct to other LDL-C-lowering therapies to …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-9642

What is NDC 71335-9642?
71335-9642 is the product NDC for Simvastatin, Simvastatin 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Simvastatin.
What is the active ingredient?
Simvastatin.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Simvastatin?
156 other product NDCs are listed under this name. See all Simvastatin 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 Simvastatin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralCoupler LLC67046-062867046-0628-03
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralCoupler LLC67046-062667046-0626-03
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralCoupler LLC67046-054267046-0542-03
SimvastatinSimvastatin 5 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-30572865-0305-0172865-0305-1072865-0305-30+1 more
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-30672865-0306-0172865-0306-1072865-0306-30+1 more
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-30772865-0307-0172865-0307-1072865-0307-30+2 more
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-30872865-0308-0172865-0308-1072865-0308-30+2 more
SimvastatinSimvastatin 80 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-30972865-0309-0172865-0309-0572865-0309-10+3 more
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-37669367-0376-0969367-0376-10
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralWestminster Pharmaceuticals, LLC69367-37469367-0374-0969367-0374-10

All 157 Simvastatin NDCs

Other NDCs under ANDA 078103

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

FDA NDC Directory listings under ANDA 078103
ProductStrengthForm · routeLabelerProduct NDC
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-464
SimvastatinSimvastatin 80 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-465
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-579
SimvastatinSimvastatin 80 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-580
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4331
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-585
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-459
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-798
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralProficient Rx LP71205-809
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-478
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-479
SimvastatinSimvastatin 5 mg/1Tablet, Film coatedOralLupin Pharmaceuticals, Inc.68180-482
SimvastatinSimvastatin 80 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-9717
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-966
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0954
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8056
SimvastatinSimvastatin 10 mg/1Tablet, Film coatedOralCoupler LLC67046-0542
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4901
SimvastatinSimvastatin 20 mg/1Tablet, Film coatedOralCoupler LLC67046-0626
SimvastatinSimvastatin 40 mg/1Tablet, Film coatedOralCoupler LLC67046-0628

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