NDC 63323-562 – Bivalirudin
Bivalirudin 250 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC63323-562
Product details
- Brand name
- Bivalirudin
- Generic name
- Bivalirudin
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA090189
- Marketed since
- October 30, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-coagulant; Direct Thrombin Inhibitor
Active ingredients
- Bivalirudin 250 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63323-562-10 | 10 VIAL, SINGLE-USE in 1 CARTON (63323-562-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE | Oct 28, 2016 |
| 63323-562-15 | 10 VIAL, SINGLE-USE in 1 CARTON (63323-562-15) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (63323-562-41) | Oct 30, 2017 |
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