Eptifibatide
- Product NDC
- 63739-923
- 11-digit product format
- 637390923
- Labeler code
- 63739
- Product ID
- 63739-923_a1cdeb24-4e68-60dd-e053-2995a90a2b23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Eptifibatide Injection
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA207864
- Marketing category
- ANDA
- Marketing start
- 2020-03-20
- 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
- 2021-12-31
- 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 |
|---|
| 63739-923-22 | 63739092322 | 1 VIAL in 1 CARTON (63739-923-22) > 100 mL in 1 VIAL | 1 vial | 2020-03-20 | 0000-00-00 | No | No | Current |