Prescription drug · ANDA
colchicine NDC 71205-687
Colchicine .6 mg/1 · Tablet · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-687-05 | 71205068705 | 5 TABLET in 1 BOTTLE (71205-687-05)Marketed from Jul 17, 2025 | |
| 71205-687-10 | 71205068710 | 10 TABLET in 1 BOTTLE (71205-687-10)Marketed from Oct 27, 2022 | |
| 71205-687-21 | 71205068721 | 21 TABLET in 1 BOTTLE (71205-687-21)Marketed from Apr 25, 2025 | |
| 71205-687-30 | 71205068730 | 30 TABLET in 1 BOTTLE (71205-687-30)Marketed from Aug 22, 2022 | |
| 71205-687-60 | 71205068760 | 60 TABLET in 1 BOTTLE (71205-687-60)Marketed from Aug 22, 2022 | |
| 71205-687-90 | 71205068790 | 90 TABLET in 1 BOTTLE (71205-687-90)Marketed from Aug 22, 2022 |
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
- Route
- Oral
- Labeler
- Proficient Rx LP
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209876
- Marketing start
- Listing expires
- Other FDA classes
- Alkaloids (Chemical structure)
- Identifiers
- Product ID 71205-687_62a7d89d-9856-446f-aaa2-962825fef0a6SPL ID 62a7d89d-9856-446f-aaa2-962825fef0a6SPL set ID 0f69b9c6-8c00-45e2-b950-34dc5ae62352RxCUI 197541UNII SML2Y3J35TUPC 0371205687304
- 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
N471205068705followed by a unit qualifier and the quantityPackage 71205-0687-05. 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 ( Error! Hyperlink reference not valid. ). 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…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 209876
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| colchicine | Colchicine .6 mg/1 | TabletOral | Dr.Reddys Laboratories, Inc. | 43598-372 |
| colchicine | Colchicine .6 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4000 |
| Colchicine | Colchicine .6 mg/1 | TabletOral | Direct Rx | 72189-331 |
| colchicine | Colchicine .6 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1738 |