Toposar
- Product NDC
- 0703-5656
- 11-digit product format
- 007035656
- Labeler code
- 0703
- Product ID
- 0703-5656_d51ca63b-e4ab-43d3-ae5b-7324f547fbc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Etoposide
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Teva Parenteral Medicines, Inc.
- Application
- ANDA074529
- Marketing category
- ANDA
- Marketing start
- 1996-08-01
- Marketing end
- 0000-00-00
- Substance
- ETOPOSIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0703-5656-01 | 00703565601 | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-5656-01) > 25 mL in 1 VIAL, MULTI-DOSE | 1996-08-01 | 0000-00-00 | No | No | Current |