NDC 63323-542 – Heparin Sodium
Heparin Sodium 10000 [USP'U]/mL · Injection, Solution · Intravenous, Subcutaneous
Product NDC63323-542
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 10000 [USP'U]/mL
Uses, dosage, side effects and warnings for Heparin Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 63323-542-13 | 25 VIAL in 1 TRAY (63323-542-13) / 1 mL in 1 VIAL (63323-542-09) | Nov 4, 2019 |
| 63323-542-14 | 25 VIAL in 1 TRAY (63323-542-14) / 5 mL in 1 VIAL (63323-542-04) | Nov 4, 2019 |
Recalls mentioning this NDC
- D-1148-2014 Mar 12, 2014 · Class II
Subpotent; 18 month time point
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