ARGATROBAN
- Product NDC
- 0078-0930
- 11-digit product format
- 000780930
- Labeler code
- 0078
- Product ID
- 0078-0930_cfd1061f-f67b-413d-979d-b58c1a1bad22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- argatroban
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Novartis Pharmaceuticals Corporation
- Application
- NDA020883
- Marketing category
- NDA
- Marketing start
- 2018-02-02
- Marketing end
- 2022-10-31
- Substance
- ARGATROBAN
- Active strength
- 100 mg/mL
- Pharmacologic classes
- Anti-coagulant [EPC],Direct Thrombin Inhibitor [EPC],Thrombin 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0078-0930-61 | 00078093061 | 1 VIAL in 1 CARTON (0078-0930-61) > 2.5 mL in 1 VIAL | 1 vial | 2018-02-02 | 0000-00-00 | No | No | Current |