NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3424Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3424Add 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
70518-3424-1705183424017051834240160 CAPSULE in 1 BOTTLE, PLASTIC (70518-3424-1)Marketed from May 23, 2025
70518-3424-2705183424027051834240290 CAPSULE in 1 BOTTLE, PLASTIC (70518-3424-2)Marketed from Jun 16, 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)
Celecoxib
Generic name (nonproprietary)
celecoxib
Active ingredients
Celecoxib — 100 mg/1
Dosage form
Capsule
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210628
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 70518-3424_5da9dee4-895d-1ee6-e063-6394a90ada5bSPL ID 5da9dee4-895d-1ee6-e063-6394a90ada5b

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

N470518342401 followed by a unit qualifier and the quantity

Package 70518-3424-01. 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

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

About NDC 70518-3424

What is NDC 70518-3424?
70518-3424 is the product NDC for Celecoxib, Celecoxib 100 mg/1 capsule, listed with the FDA by REMEDYREPACK INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Celecoxib.
What is the active ingredient?
Celecoxib.
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 Celecoxib?
230 other product NDCs are listed under this name. See all Celecoxib 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 Celecoxib NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CelecoxibCelecoxib 200 mg/1CapsuleOralDirect_Rx72189-69572189-0695-3072189-0695-60
CelecoxibCelecoxib 100 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-94260760-0942-60
CelecoxibCelecoxib 100 mg/1CapsuleOralDirect_Rx72189-68572189-0685-6072189-0685-72
CelecoxibCelecoxib 200 mg/1CapsuleOralREMEDYREPACK INC.70518-472670518-4726-00
CelecoxibCelecoxib 200 mg/1CapsuleOralSt. Mary's Medical Park Pharmacy60760-95860760-0958-1560760-0958-3060760-0958-60
CelecoxibCelecoxib 100 mg/1CapsuleOralCardinal Health 107, LLC55154-016055154-0160-00
CelecoxibCelecoxib 400 mg/1CapsuleOralREMEDYREPACK INC.70518-461970518-4619-00
CelecoxibCelecoxib 100 mg/1CapsuleOralMajor Pharmaceuticals0904-755000904-7550-61
CelecoxibCelecoxib 200 mg/1CapsuleOralMajor Pharmaceuticals0904-755100904-7551-61
CelecoxibCelecoxib 100 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-96423155-0964-0123155-0964-05

All 231 Celecoxib NDCs

Other NDCs under ANDA 210628

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

FDA NDC Directory listings under ANDA 210628
ProductStrengthForm · routeLabelerProduct NDC
CelecoxibCelecoxib 50 mg/1CapsuleOralUmedica Laboratories USA Inc.60290-016
CelecoxibCelecoxib 100 mg/1CapsuleOralUmedica Laboratories USA Inc.60290-017
CelecoxibCelecoxib 200 mg/1CapsuleOralUmedica Laboratories USA Inc.60290-018
CelecoxibCelecoxib 400 mg/1CapsuleOralUmedica Laboratories USA Inc.60290-019
CelecoxibCelecoxib 100 mg/1CapsuleOralBryant Ranch Prepack71335-2019
CelecoxibCelecoxib 200 mg/1CapsuleOralBryant Ranch Prepack72162-2357
CelecoxibCelecoxib 50 mg/1CapsuleOralNIVAGEN PHARMACEUTICALS, INC.75834-236
CelecoxibCelecoxib 100 mg/1CapsuleOralNIVAGEN PHARMACEUTICALS, INC.75834-237
CelecoxibCelecoxib 200 mg/1CapsuleOralNIVAGEN PHARMACEUTICALS, INC.75834-238
CelecoxibCelecoxib 400 mg/1CapsuleOralNIVAGEN PHARMACEUTICALS, INC.75834-239
CelecoxibCelecoxib 200 mg/1CapsuleOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0281
CelecoxibCelecoxib 100 mg/1CapsuleOralPHOENIX RX LLC85509-1237

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