NDC codes

FDA NDC Directory
Product NDC (as listed)60429-312Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60429-0312Add 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
60429-312-0160429031201100 TABLET, FILM COATED in 1 BOTTLE (60429-312-01)Marketed from Jul 18, 2011

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)
Etodolac
Generic name (nonproprietary)
etodolac
Active ingredients
Etodolac500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075074
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 60429-312_586539b9-9b0f-ec17-e063-6294a90a3328SPL ID 586539b9-9b0f-ec17-e063-6294a90a3328SPL set ID cf17926c-ed90-4fd0-80af-ccee084075e8RxCUI 197684, 197685, 197686, 199390UNII 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

N460429031201 followed by a unit qualifier and the quantity

Package 60429-0312-01. 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 capsules and tablets and other treatment options before deciding to use etodolac capsules and tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Etodolac Capsules and Tablets are indicated: For acute and long-term use in the management of signs and symptoms of the following: Osteoarthritis Rheumatoid arthritis For the management of acute pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075074

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

FDA NDC Directory listings under ANDA 075074
ProductStrengthForm · routeLabelerProduct NDC
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-779
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-795
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-816
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-311
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4291
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-859
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0551
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.51672-4018
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralSun Pharmaceutical Industries, Inc.51672-4036
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8673
EtodolacEtodolac 400 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1958
EtodolacEtodolac 500 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1489

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Etodolac NDC 60429-312 | Med-Code