Ontruzant
- Product NDC
- 0006-5034
- 11-digit product format
- 000065034
- Labeler code
- 0006
- Product ID
- 0006-5034_419c4f97-e6d6-4bed-9014-a69a39d2149f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ontruzant
- Dosage form
- KIT
- Route
- INTRAVENOUS
- Labeler
- Merck Sharp & Dohme Corp.
- Application
- BLA761100
- Marketing category
- BLA
- Marketing start
- 2020-04-15
- Marketing end
- 2023-09-30
- Active strength
- 0
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0006-5034-02 | 00006503402 | 1 KIT in 1 CARTON (0006-5034-02) * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE * 1 INJECTION, SOLUTION in 1 VIAL | 1 kit | 2020-04-15 | 0000-00-00 | No | No | Current |