NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4542Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4542Add 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
70518-4542-0705184542007051845420060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4542-0)Marketed from Dec 30, 2025

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)
Etodolac
Generic name (nonproprietary)
etodolac
Active ingredients
Etodolac — 400 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076004
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 70518-4542_5b9c65c4-250b-412e-e063-6294a90a06a9SPL ID 5b9c65c4-250b-412e-e063-6294a90a06a9

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

N470518454200 followed by a unit qualifier and the quantity

Package 70518-4542-00. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70518-4542

What is NDC 70518-4542?
70518-4542 is the product NDC for Etodolac, Etodolac 400 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Etodolac.
What is the active ingredient?
Etodolac.
Who is the labeler?
REMEDYREPACK INC., NDC labeler code 70518. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Etodolac?
100 other product NDCs are listed under this name. See all Etodolac 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 Etodolac NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-46159651-0461-01
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-46259651-0462-01
etodolacEtodolac 400 mg/1TabletOralIpca Laboratories Limited83980-02983980-0029-0183980-0029-1083980-0029-13
etodolacEtodolac 500 mg/1TabletOralIpca Laboratories Limited83980-03083980-0030-0183980-0030-0583980-0030-13
etodolacEtodolac 300 mg/1CapsuleOralA-S Medication Solutions50090-803750090-8037-01
etodolacEtodolac 200 mg/1CapsuleOralIpca Laboratories Limited83980-03183980-0031-0183980-0031-0583980-0031-13
etodolacEtodolac 300 mg/1CapsuleOralIpca Laboratories Limited83980-03283980-0032-0183980-0032-0583980-0032-13
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-055180425-0551-01
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-884668788-8846-0168788-8846-0268788-8846-03+2 more
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-429170518-4291-00

All 101 Etodolac NDCs

Other NDCs under ANDA 076004

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

FDA NDC Directory listings under ANDA 076004
ProductStrengthForm · routeLabelerProduct NDC
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-578
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-671
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-856
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralMedsource Pharmaceuticals45865-206
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1790
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralApotex Corp.60505-0041
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralApotex Corp.60505-0102
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralSt. Marys Medical Park Pharmacy60760-552
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralProficient Rx LP63187-736
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-8805
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8846
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3845
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralProficient Rx LP71205-467
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0126
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0399
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-804
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-538
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0190

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