NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0181Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0181Add 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
80425-0181-1804250181018042501810130 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0181-1)Marketed from Mar 13, 2003

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 ERSuffix: ER
Generic name (nonproprietary)
etodolac
Active ingredients
Etodolac — 600 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076174
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 80425-0181_2a99a670-af34-299d-e063-6294a90a05d2SPL ID 2a99a670-af34-299d-e063-6294a90a05d2SPL set ID d294d541-3049-6bfe-e053-2995a90a23eaRxCUI 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

N480425018101 followed by a unit qualifier and the quantity

Package 80425-0181-01. 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: For relief of signs and symptoms of juvenile arthritis For relief of the signs and symptoms of rheumatoid arthritis For relief of the signs and symptoms of osteoarthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0181

What is NDC 80425-0181?
80425-0181 is the product NDC for Etodolac ER (etodolac), Etodolac 600 mg/1 tablet, extended release, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Etodolac ER (Etodolac).
What is the active ingredient?
Etodolac.
Who is the labeler?
Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. 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 ER?
1 other product NDC are listed under this name. See all Etodolac ER 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 ER NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Etodolac ERetodolacEtodolac 600 mg/1Tablet, Extended releaseOralAdvanced Rx Pharmacy of Tennessee, LLC80425-012680425-0126-01

Other NDCs under ANDA 076174

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

FDA NDC Directory listings under ANDA 076174
ProductStrengthForm · routeLabelerProduct NDC
EtodolacEtodolac 400 mg/1Tablet, Extended releaseOralNORTHSTAR RX LLC16714-497
EtodolacEtodolac 500 mg/1Tablet, Extended releaseOralNORTHSTAR RX LLC16714-498
EtodolacEtodolac 600 mg/1Tablet, Extended releaseOralNORTHSTAR RX LLC16714-499
EtodolacEtodolac 400 mg/1Tablet, Extended releaseOralTaSun Pharmaceutical Industries, Inc.51672-4051
EtodolacEtodolac 500 mg/1Tablet, Extended releaseOralTaSun Pharmaceutical Industries, Inc.51672-4052
EtodolacEtodolac 600 mg/1Tablet, Extended releaseOralTaSun Pharmaceutical Industries, Inc.51672-4053
EtodolacEtodolac 400 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.60429-313
EtodolacEtodolac 500 mg/1Tablet, Extended releaseOralGolden State Medical Supply, Inc.60429-314
EtodolacEtodolac 400 mg/1Tablet, Extended releaseOralProficient Rx LP63187-793
Etodolac ERetodolacEtodolac 600 mg/1Tablet, Extended releaseOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0126

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