ETOPOPHOS
- Product NDC
- 0015-3404
- 11-digit product format
- 000153404
- Labeler code
- 0015
- Product ID
- 0015-3404_f781e9d9-650f-4d32-b78c-0660a0ea743a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- etoposide phosphate
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- E.R. Squibb & Sons, L.L.C.
- Application
- NDA020457
- Marketing category
- NDA
- Marketing start
- 2009-06-01
- Marketing end
- 2021-04-30
- Substance
- ETOPOSIDE PHOSPHATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0015-3404-20 | 00015340420 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0015-3404-20) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 2009-06-01 | 2021-04-30 | No | No | Current |