Prescription drug · ANDA
Pazopanib NDC 51407-872
Pazopanib 200 mg/1 · Tablet · Oral · Golden State Medical Supply, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51407-872-12 | 5140708721251407087212 | 120 TABLET in 1 BOTTLE (51407-872-12)Marketed from Jan 8, 2024 |
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)
- Pazopanib
- Generic name (nonproprietary)
- pazopanib
- Active ingredients
- Pazopanib — 200 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Golden State Medical Supply, Inc.NDC labeler code 51407
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 217713
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C8 Inhibitors (Mechanism)Cytochrome P450 2D6 Inhibitors (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)Protein Kinase Inhibitors (Mechanism)
- Identifiers
- Product ID 51407-872_445b5e3e-5de0-323d-e063-6394a90a5faeSPL ID 445b5e3e-5de0-323d-e063-6394a90a5faeSPL set ID 115eb5bb-1403-fb3d-e063-6394a90ad320RxCUI 867502UNII 7RN5DR86CK
- Pharmacologic class
- Kinase Inhibitor
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
N451407087212followed by a unit qualifier and the quantityPackage 51407-0872-12. 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)
Pazopanib tablets are a kinase inhibitor indicated for the treatment of adults with: advanced renal cell carcinoma (RCC). ( 1.1 ) advanced soft tissue sarcoma (STS) who have received prior chemotherapy. ( 1.2 ) Limitations of Use: The efficacy of pazopanib tablets for the treatment of patients with adipocytic soft tissue sarcoma or gastrointestinal stromal tumors has not been demonstrated. 1.1 Renal Cell Carcinoma Pazopanib tablets are indicated for the treatment of adults with advanced renal cell carcinoma (RCC). 1.2 Soft Tissue Sarcoma Pazopanib tablets are indicated for the treatment of adults with advanced soft tissue sarcoma (STS) who have received prior chemotherapy. Limitations of Use…
Excerpt only. Read the full label for complete information.
About NDC 51407-872
- What is NDC 51407-872?
- 51407-872 is the product NDC for Pazopanib, Pazopanib 200 mg/1 tablet, listed with the FDA by Golden State Medical Supply, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pazopanib.
- What is the active ingredient?
- Pazopanib.
- Who is the labeler?
- Golden State Medical Supply, Inc., NDC labeler code 51407. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pazopanib?
- 7 other product NDCs are listed under this name. See all Pazopanib NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Pazopanib products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| pazopanibpazopanib hydrochloride | Pazopanib hydrochloride 400 mg/1 | Tablet, Film coatedOral | Torrent Pharmaceuticals Limited | 13668-735 | 13668-0735-3013668-0735-6013668-0735-90 |
| Pazopanib | Pazopanib hydrochloride 200 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-582 | 59651-0582-0859651-0582-3059651-0582-90 |
| pazopanibpazopanib hydrochloride | Pazopanib hydrochloride 200 mg/1 | Tablet, Film coatedOral | Novugen Pharma (USA) LLC. | 82293-022 | 82293-0022-10 |
| Pazopanib | Pazopanib hydrochloride 200 mg/1 | Tablet, Film coatedOral | AvKARE | 42291-939 | 42291-0939-12 |
| Pazopanib | Pazopanib hydrochloride 200 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals, Inc. | 0480-4184 | 00480-4184-89 |
| Pazopanib | Pazopanib hydrochloride 200 mg/1 | Tablet, Film coatedOral | SUN PHARMACEUTICAL INDUSTRIES, INC. | 63304-116 | 63304-0116-1363304-0116-30 |
| Pazopanib | Pazopanib 200 mg/1 | TabletOral | Apotex Corp. | 60505-4779 | 60505-4779-0560505-4779-07 |
Other NDCs under ANDA 217713
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 |
|---|---|---|---|---|
| Pazopanib | Pazopanib 200 mg/1 | TabletOral | Apotex Corp. | 60505-4779 |