Prescription drug · ANDA
Temozolomide NDC 31722-415
Temozolomide 180 mg/1 · Capsule · Oral · Camber Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 31722-415-14 | 31722041514 | 14 CAPSULE in 1 BOTTLE (31722-415-14)Marketed from Aug 23, 2024 | |
| 31722-415-31 | 31722041531 | 5 CAPSULE in 1 BOTTLE (31722-415-31)Marketed from Aug 23, 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)
- Temozolomide
- Generic name (nonproprietary)
- temozolomide
- Active ingredients
- Temozolomide — 180 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Camber Pharmaceuticals, Inc.NDC labeler code 31722
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 210030
- Marketing start
- Listing expires
- Other FDA classes
- Alkylating Activity (Mechanism)
- Identifiers
- Product ID 31722-415_24d38de8-4acf-bdac-e063-6394a90ad431SPL ID 24d38de8-4acf-bdac-e063-6394a90ad431SPL set ID 78c12889-c837-40c1-8f85-4d048008ad29RxCUI 313209, 313210, 313211, 317160, 700883, 700885UNII YF1K15M17YUPC 0331722415316, 0331722414319, 0331722413312, 0331722411318, 0331722412315, 0331722416313
- Pharmacologic class
- Alkylating Drug
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
N431722041514followed by a unit qualifier and the quantityPackage 31722-0415-14. 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)
Temozolomide capsule is an alkylating drug indicated for the treatment of adults with: • Newly diagnosed glioblastoma concomitantly with radiotherapy and then as maintenance treatment. ( 1.1 ) • Anaplastic astrocytoma. ( 1.2 ) o Adjuvant treatment of adults with newly diagnosed anaplastic astrocytoma. ( 1.2 ) o Treatment of adults with refractory anaplastic astrocytoma. ( 1.2 ) 1.1 Newly Diagnosed Glioblastoma Temozolomide capsules are indicated for the treatment of adults with newly diagnosed glioblastoma, concomitantly with radiotherapy and then as maintenance treatment. 1.2 Anaplastic Astrocytoma Temozolomidecapsules are indicated for the: •adjuvant treatment of adults with newly diagnose…
Excerpt only. Read the full label for complete information.
About NDC 31722-415
- What is NDC 31722-415?
- 31722-415 is the product NDC for Temozolomide, Temozolomide 180 mg/1 capsule, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Temozolomide.
- What is the active ingredient?
- Temozolomide.
- Who is the labeler?
- Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Temozolomide?
- 63 other product NDCs are listed under this name. See all Temozolomide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Temozolomide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Temozolomide | Temozolomide 100 mg/1 | CapsuleOral | OPKO Pharmaceuticals, LLC | 70301-2005 | 70301-2005-0170301-2005-02 |
| Temozolomide | Temozolomide 140 mg/1 | CapsuleOral | OPKO Pharmaceuticals, LLC | 70301-2007 | 70301-2007-0170301-2007-02 |
| Temozolomide | Temozolomide 180 mg/1 | CapsuleOral | OPKO Pharmaceuticals, LLC | 70301-2009 | 70301-2009-0170301-2009-02 |
| Temozolomide | Temozolomide 250 mg/1 | CapsuleOral | OPKO Pharmaceuticals, LLC | 70301-2011 | 70301-2011-01 |
| Temozolomide | Temozolomide 5 mg/1 | CapsuleOral | CivicaScript LLC | 82249-404 | 82249-0404-0582249-0404-14 |
| Temozolomide | Temozolomide 20 mg/1 | CapsuleOral | CivicaScript LLC | 82249-406 | 82249-0406-0582249-0406-14 |
| Temozolomide | Temozolomide 100 mg/1 | CapsuleOral | CivicaScript LLC | 82249-408 | 82249-0408-0582249-0408-14 |
| Temozolomide | Temozolomide 140 mg/1 | CapsuleOral | CivicaScript LLC | 82249-410 | 82249-0410-0582249-0410-14 |
| Temozolomide | Temozolomide 180 mg/1 | CapsuleOral | CivicaScript LLC | 82249-412 | 82249-0412-0582249-0412-14 |
| Temozolomide | Temozolomide 250 mg/1 | CapsuleOral | CivicaScript LLC | 82249-414 | 82249-0414-05 |
Other NDCs under ANDA 210030
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 |
|---|---|---|---|---|
| Temozolomide | Temozolomide 5 mg/1 | CapsuleOral | Camber Pharmaceuticals, Inc. | 31722-411 |
| Temozolomide | Temozolomide 20 mg/1 | CapsuleOral | Camber Pharmaceuticals, Inc. | 31722-412 |
| Temozolomide | Temozolomide 100 mg/1 | CapsuleOral | Camber Pharmaceuticals, Inc. | 31722-413 |
| Temozolomide | Temozolomide 140 mg/1 | CapsuleOral | Camber Pharmaceuticals, Inc. | 31722-414 |
| Temozolomide | Temozolomide 250 mg/1 | CapsuleOral | Camber Pharmaceuticals, Inc. | 31722-416 |