NDC 63323-145 – Floxuridine
Floxuridine 500 mg/5mL · Injection, Powder, Lyophilized, For Solution · Intra-arterial
Product NDC63323-145
Product details
- Brand name
- Floxuridine
- Generic name
- Floxuridine
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intra-arterial
- Marketing category
- ANDA · ANDA075837
- Marketed since
- March 15, 2001
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antimetabolite
Active ingredients
- Floxuridine 500 mg/5mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 63323-145-07 | 1 VIAL in 1 CARTON (63323-145-07) / 5 mL in 1 VIAL | Mar 15, 2001 |
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