NDC 0409-4332 – Vancomycin Hydrochloride
Vancomycin Hydrochloride 500 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC0409-4332
Product details
- Brand name
- Vancomycin Hydrochloride
- Generic name
- Vancomycin Hydrochloride
- Labeler
- Hospira, Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA062911
- Marketed since
- April 30, 2005
- Listing expires
- December 31, 2027
- Pharmacologic class
- Glycopeptide Antibacterial
Active ingredients
- Vancomycin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Vancomycin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0409-4332-01 | 10 VIAL in 1 TRAY (0409-4332-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0409-4332-11) | Apr 30, 2005 |
Recalls mentioning this NDC
- D-0184-2023 Feb 1, 2023 · Class I
Presence of Particulate Matter: Glass particulate matter detected in injectable. - D-0123-2018 Dec 27, 2017 · Class I
Presence of Particulate Matter: glass particulate found in vial - D-0390-2015 Feb 25, 2015 · Class II
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit. - D-0387-2015 Feb 25, 2015 · Class II
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit. - D-0254-2015 Nov 26, 2014 · Class III
Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
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