Eptifibatide
- Product NDC
- 0338-9559
- 11-digit product format
- 003389559
- Labeler code
- 0338
- Product ID
- 0338-9559_c8051921-bbb9-4a3b-a930-f179dce2181b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eptifibatide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA208554
- Marketing category
- ANDA
- Marketing start
- 2019-02-01
- Marketing end
- 0000-00-00
- Substance
- EPTIFIBATIDE
- Active strength
- 200 mg/100mL
- Pharmacologic classes
- Decreased Platelet Aggregation [PE], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0338-9559-20 | 00338955920 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0338-9559-20) > 100 mL in 1 VIAL, SINGLE-DOSE | 2019-02-01 | 0000-00-00 | No | No | Current |