Prescription drug · ANDA
Probenecid and Colchicine NDC 50742-263
Probenecid 500 mg/1; Colchicine .5 mg/1 · Tablet · Oral · Ingenus Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50742-263-01 | 5074202630150742026301 | 100 TABLET in 1 BOTTLE (50742-263-01)Marketed from May 16, 2019 |
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)
- Probenecid and Colchicine
- Generic name (nonproprietary)
- probenecid and colchicine
- Active ingredients
- Probenecid — 500 mg/1Colchicine — .5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Ingenus Pharmaceuticals, LLCNDC labeler code 50742
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 040618
- Marketing start
- Listing expires
- Other FDA classes
- Alkaloids (Chemical structure)
- Identifiers
- Product ID 50742-263_8f0d4438-1ba8-419c-864f-b95cb0b006efSPL ID 8f0d4438-1ba8-419c-864f-b95cb0b006efSPL set ID b85d3e27-70ff-4533-b463-410e4fb23813RxCUI 198153UNII PO572Z7917, SML2Y3J35TUPC 0350742263011
- 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
N450742026301followed by a unit qualifier and the quantityPackage 50742-0263-01. 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 .
Indications (excerpt from the label)
INDICATIONS AND USAGE For the treatment of chronic gouty arthritis when complicated by frequent, recurrent acute attacks of gout.
Excerpt only. Read the full label for complete information.
About NDC 50742-263
- What is NDC 50742-263?
- 50742-263 is the product NDC for Probenecid and Colchicine, Probenecid 500 mg/1; Colchicine .5 mg/1 tablet, listed with the FDA by Ingenus Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Probenecid and Colchicine.
- What is the active ingredient?
- Probenecid, Colchicine.
- Who is the labeler?
- Ingenus Pharmaceuticals, LLC, NDC labeler code 50742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Probenecid and Colchicine?
- 2 other product NDCs are listed under this name. See all Probenecid and Colchicine NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Probenecid and Colchicine products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Probenecid and Colchicine | Probenecid 500 mg/1; Colchicine .5 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4644 | 70518-4644-00 |
| Probenecid and Colchicine | Probenecid 500 mg/1; Colchicine .5 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 16571-832 | 16571-0832-01 |