NDC 63323-540 – Heparin Sodium
Heparin Sodium 1000 [USP'U]/mL · Injection, Solution · Intravenous, Subcutaneous
Product NDC63323-540
Product details
- Brand name
- Heparin Sodium
- Generic name
- Heparin Sodium
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous, Subcutaneous
- Marketing category
- NDA · NDA017029
- Marketed since
- November 4, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-coagulant; Unfractionated Heparin
Active ingredients
- Heparin Sodium 1000 [USP'U]/mL
Uses, dosage, side effects and warnings for Heparin Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 63323-540-13 | 25 VIAL in 1 TRAY (63323-540-13) / 1 mL in 1 VIAL (63323-540-03) | Nov 4, 2019 |
| 63323-540-15 | 25 VIAL in 1 TRAY (63323-540-15) / 10 mL in 1 VIAL (63323-540-05) | Nov 4, 2019 |
| 63323-540-36 | 25 VIAL in 1 TRAY (63323-540-36) / 30 mL in 1 VIAL (63323-540-33) | Nov 4, 2019 |
| 63323-540-67 | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-540-67) / 10 mL in 1 VIAL, MULTI-DOSE (63323-540-07) | Mar 25, 2020 |
Recalls mentioning this NDC
- D-1148-2014 Mar 12, 2014 · Class II
Subpotent; 18 month time point
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