NDC codes

FDA NDC Directory
Product NDC (as listed)72789-572Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0572Add 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
72789-572-30727890572307278905723030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-572-30)Marketed from May 20, 2026

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)
Colchicine
Generic name (nonproprietary)
colchicine
Active ingredients
Colchicine — .6 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208993
Marketing start
Listing expires
Other FDA classes
Alkaloids (Chemical structure)
Identifiers
Product ID 72789-572_5245af45-77cc-c95f-e063-6294a90a24f7SPL ID 5245af45-77cc-c95f-e063-6294a90a24f7SPL set ID 68d4bf2b-8e2c-4621-aa08-463f43e253c3RxCUI 197541UNII SML2Y3J35T
Pharmacologic class
Alkaloid

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

N472789057230 followed by a unit qualifier and the quantity

Package 72789-0572-30. 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 .

Indications (excerpt from the label)

Colchicine tablets are an alkaloid indicated for: • Prophylaxis and treatment of gout flares in adults (1.1). • Familial Mediterranean fever (FMF) in adults and children 4 years or older (1.2). 1.1 Gout Flares Colchicine tablets are indicated for prophylaxis and the treatment of acute gout flares. • Prophylaxis of Gout Flares: Colchicine tablets are indicated for prophylaxis of gout flares. • Treatment of Gout Flares: Colchicine tablets are indicated for treatment of acute gout flares when taken at the first sign of a flare. 1.2 Familial Mediterranean Fever (FMF) Colchicine tablets are indicated in adults and children four years or older for treatment of familial Mediterranean fever (FMF).…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72789-572

What is NDC 72789-572?
72789-572 is the product NDC for Colchicine, Colchicine .6 mg/1 tablet, film coated, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Colchicine.
What is the active ingredient?
Colchicine.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Colchicine?
48 other product NDCs are listed under this name. See all Colchicine 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 Colchicine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ColchicineColchicine .6 mg/1Tablet, Film coatedOralDirect_Rx72189-68772189-0687-03
colchicineColchicine .6 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-83960760-0839-10
ColchicineColchicine .6 mg/1CapsuleOralMicro Labs Limited42571-34142571-0341-0142571-0341-1042571-0341-30
ColchicineColchicine .6 mg/1CapsuleOralCoupler LLC67046-163467046-1634-03
ColchicineColchicine .6 mg/1CapsuleOralCoupler LLC67046-088967046-0889-03
ColchicineColchicine .6 mg/1CapsuleOralCamber Pharmaceuticals, Inc.31722-09931722-0099-0131722-0099-1031722-0099-30
ColchicineColchicine .6 mg/1CapsuleOralGranules Pharmaceutical Inc.70010-00170010-0001-0170010-0001-0370010-0001-10
ColchicineColchicine .6 mg/1CapsuleOralBryant Ranch Prepack71335-270371335-2703-0171335-2703-0271335-2703-03+5 more
colchicineColchicine .6 mg/1TabletOralREMEDYREPACK INC.70518-400070518-4000-01
ColchicineColchicine .6 mg/1CapsuleOralPar Health USA, LLC0254-046000254-0460-01

All 49 Colchicine NDCs

Other NDCs under ANDA 208993

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

FDA NDC Directory listings under ANDA 208993
ProductStrengthForm · routeLabelerProduct NDC
ColchicineColchicine .6 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-899
ColchicineColchicine .6 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2791
ColchicineColchicine .6 mg/1Tablet, Film coatedOralDirect_Rx72189-687

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