NDC codes

FDA NDC Directory
Product NDC (as listed)63629-8598Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-8598Add 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
63629-8598-1636298598016362985980130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-8598-1)Marketed from Jun 22, 2021

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 — 600 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 63629
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091134
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 63629-8598_24f87f5a-05f7-4825-b5d5-344596325f0cSPL ID 24f87f5a-05f7-4825-b5d5-344596325f0cSPL set ID 1e4824cc-4d52-4f20-9674-cfcb9ee66574RxCUI 310247UNII 2M36281008

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

N463629859801 followed by a unit qualifier and the quantity

Package 63629-8598-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Carefully consider the potential benefits and risks of etodolac extended-release tablets and other treatment options before deciding to use etodolac extended-release tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Etodolac extended-release tablets are indicated:

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-8598

What is NDC 63629-8598?
63629-8598 is the product NDC for Etodolac, Etodolac 600 mg/1 tablet, film coated, extended release, listed with the FDA by Bryant Ranch Prepack. 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?
Bryant Ranch Prepack, NDC labeler code 63629. 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 coatedOralREMEDYREPACK INC.70518-454270518-4542-00
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

All 101 Etodolac NDCs

Other NDCs under ANDA 091134

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

FDA NDC Directory listings under ANDA 091134
ProductStrengthForm · routeLabelerProduct NDC
EtodolacEtodolac 500 mg/1Tablet, Film coated, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-298
EtodolacEtodolac 400 mg/1Tablet, Film coated, Extended releaseOralProficient Rx LP63187-374
EtodolacEtodolac 400 mg/1Tablet, Film coated, Extended releaseOralZydus Lifesciences Limited65841-777
EtodolacEtodolac 500 mg/1Tablet, Film coated, Extended releaseOralZydus Lifesciences Limited65841-778
EtodolacEtodolac 600 mg/1Tablet, Film coated, Extended releaseOralZydus Lifesciences Limited65841-779
EtodolacEtodolac 400 mg/1Tablet, Film coated, Extended releaseOralNuCare Pharmaceuticals, Inc.68071-3731
EtodolacEtodolac 400 mg/1Tablet, Film coated, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-271
EtodolacEtodolac 500 mg/1Tablet, Film coated, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-272
EtodolacEtodolac 600 mg/1Tablet, Film coated, Extended releaseOralZydus Pharmaceuticals USA Inc.68382-273
EtodolacEtodolac 600 mg/1Tablet, Film coated, Extended releaseOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0381

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in