Prescription drug · ANDA
Etoposide NDC 71288-176
Etoposide 20 mg/mL · Injection, Solution, Concentrate · Intravenous · Meitheal Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71288-176-25 | 71288017625 | 1 VIAL, MULTI-DOSE in 1 CARTON (71288-176-25) / 25 mL in 1 VIAL, MULTI-DOSEMarketed from Feb 1, 2025 |
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)
- Etoposide
- Generic name (nonproprietary)
- etoposide
- Active ingredients
- Etoposide — 20 mg/mL
- Dosage form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 074529
- Marketing start
- Listing expires
- Other FDA classes
- Topoisomerase Inhibitors (Mechanism)
- Identifiers
- Product ID 71288-176_737a9d5b-1260-408a-a117-b0b3aeba6ad4SPL ID 737a9d5b-1260-408a-a117-b0b3aeba6ad4SPL set ID 50491106-dddd-4efd-bd83-060e7947a244RxCUI 310248UNII 6PLQ3CP4P3
- Pharmacologic class
- Topoisomerase 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- Administration
Drug administration (CPT 96360–96549)
When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.
- NDC on a medical claim
N471288017625followed by a unit qualifier and the quantityPackage 71288-0176-25. 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)
INDICATIONS AND USAGE Etoposide Injection is indicated in the management of the following neoplasms: Refractory Testicular Tumors Etoposide Injection in combination therapy with other approved chemotherapeutic agents in patients with refractory testicular tumors who have already received appropriate surgical, chemotherapeutic, and radiotherapeutic therapy. Small Cell Lung Cancer Etoposide Injection and/or capsules in combination with other approved chemotherapeutic agents as first line treatment in patients with small cell lung cancer.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 074529
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 |
|---|---|---|---|---|
| Etoposide | Etoposide 20 mg/mL | Injection, Solution, ConcentrateIntravenous | BluePoint Laboratories | 68001-681 |
| Etoposide | Etoposide 20 mg/mL | Injection, Solution, ConcentrateIntravenous | BluePoint Laboratories | 68001-682 |
| Etoposide | Etoposide 20 mg/mL | Injection, Solution, ConcentrateIntravenous | BluePoint Laboratories | 68001-683 |
| Etoposide | Etoposide 20 mg/mL | Injection, Solution, ConcentrateIntravenous | Meitheal Pharmaceuticals Inc. | 71288-175 |
| Etoposide | Etoposide 20 mg/mL | Injection, Solution, ConcentrateIntravenous | Meitheal Pharmaceuticals Inc. | 71288-177 |