Eptifibatide
- Product NDC
- 17478-903
- 11-digit product format
- 174780903
- Labeler code
- 17478
- Product ID
- 17478-903_94ce9e23-cb13-4a44-aaab-a366edfb69f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eptifibatide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA204589
- Marketing category
- ANDA
- Marketing start
- 2017-04-18
- Marketing end
- 0000-00-00
- Substance
- EPTIFIBATIDE
- Active strength
- 1 mg/mL
- 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 |
|---|
| 17478-903-90 | 17478090390 | 1 VIAL, SINGLE-DOSE in 1 CARTON (17478-903-90) > 100 mL in 1 VIAL, SINGLE-DOSE | 2017-04-18 | 0000-00-00 | No | No | Current |