Glycopeptide Antibacterial
Who makes generic Vancomycin?
30 companies sell Vancomycin in the U.S. under their own name, and 5 repackagers rebottle it for pharmacies.
Their labels name factories in the United States, India, Denmark, Taiwan, China, Brazil and Poland.
Which one is yours? Look for the NDC number on your bottle or pharmacy label and enter it below. The first two parts of the number identify the company and product.
Companies and their factories
injection, powder, lyophilized, for solution · 1 g per 20 mL, 5 g per 100 mL, 10 g per 100 mL, 500 mg per 10 mL, 750 mg per 15 mL ·
NDC 63323-284, 63323-314, 63323-295, 63323-221, 63323-203
- Fresenius Kabi USA, LLC Grand Island, NY, United States
Makes it and tests it Problems found, fixed voluntarily last FDA inspection Oct 2023
- Fresenius Kabi USA, LLC Melrose Park, IL, United States
Makes it and tests it Problems found, fixed voluntarily last FDA inspection Aug 2023
- Gland Pharma Limited Hyderabad, India
Makes it, makes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jul 2024
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jun 2023
- Xellia Pharmaceuticals ApS Copenhagen S, Denmark
Makes it, makes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Dec 2025
injection, powder, lyophilized, for solution · 1 g, 1 g per 10 mL, 5 g per 100 mL, 10 g per 100 mL, 500 mg per 10 mL, 500 mg per 5 mL ·
NDC 72572-029, 72572-801, 72572-805, 72572-803, 72572-105, 72572-207
- Hospira, Inc. McPherson, KS, United States
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jan 2025
- Xellia Pharmaceuticals ApS Copenhagen S, Denmark
Makes it, makes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Dec 2025
injection, powder, lyophilized, for solution · 1 g per 20 mL, 1.25 g, 1.5 g, 5 g per 100 mL, 10 g per 100 mL, 500 mg per 10 mL ·
NDC 68083-144, 68083-596, 68083-597, 68083-570, 68083-569, 68083-143 and 1 more
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jul 2024
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jun 2023
injection, powder, lyophilized, for solution · 1 g per 20 mL, 1.25 g, 1.5 g, 5 g per 100 mL, 10 g per 100 mL, 500 mg per 10 mL ·
NDC 68462-956, 68462-478, 68462-479, 68462-958, 68462-957, 68462-955 and 1 more
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jul 2024
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jun 2023
injection, powder, lyophilized, for solution · 1 g per 20 mL, 5 g per 100 mL, 10 g per 95 mL, 500 mg per 10 mL, 750 mg per 15 mL ·
NDC 71288-023, 71288-026, 71288-025, 71288-022, 71288-024
injection, powder, for solution, injection, powder, lyophilized, for solution, injection, solution · 1 g, 1 g per 200 mL, 1.25 g per 250 mL, 1.5 g per 300 mL, 1.75 g per 350 mL, 2 g per 400 mL ·
NDC 70594-046, 70594-123, 70594-042, 70594-057, 70594-043, 70594-058 and 7 more
- Xellia Pharmaceuticals ApS Copenhagen S, Denmark
Makes it, makes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Dec 2025
injection, powder, lyophilized, for solution · 1 g per 20 mL, 1.25 g per 25 mL, 1.5 g per 30 mL, 5 g, 10 g, 500 mg per 10 mL ·
NDC 55150-204, 55150-471, 55150-472, 55150-206, 55150-205, 55150-203
injection, solution · 1 g per 200 mL, 1.25 g per 250 mL, 1.50 g per 300 mL, 500 mg per 100 mL, 750 mg per 150 mL ·
NDC 0338-3552, 0338-3583, 0338-0122, 0338-0124, 0338-3551, 0338-3581 and 2 more
- Baxter Healthcare Corporation Round Lake, IL, United States
Makes it, tests it, packages it, labels it and sterilizes it Serious problems, FDA action last FDA inspection Apr 2026
injection, powder, lyophilized, for solution · 1 g per 20 mL, 500 mg per 10 mL ·
NDC 31722-211, 31722-210
injection, powder, lyophilized, for solution, injection, solution, injection, powder, for solution · 1 g, 1 g per 200 mL, 1.25 g, 1.25 g per 250 mL, 1.5 g, 1.5 g per 300 mL ·
NDC 0143-9357, 0143-9472, 0143-9152, 0143-9466, 0143-9153, 0143-9469 and 15 more
injection, powder, lyophilized, for solution · 1 g, 1.5 g, 500 mg, 500 mg per 10 mL, 500 mg per 5 mL, 750 mg ·
NDC 0409-6533, 0409-3515, 0409-4332, 0409-6509, 0409-1319, 0409-5017 and 1 more
- Hospira, Inc. McPherson, KS, United States
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jan 2025
injection, powder, lyophilized, for solution · 1 g per 20 mL, 500 mg per 10 mL ·
NDC 43538-810, 43538-805
- Eurofarma Laboratorios S.A. Itapevi, Brazil
Makes it, tests it, packages it, labels it and sterilizes it Problems found, fixed voluntarily last FDA inspection Sep 2022
injection, powder, lyophilized, for solution · 100 g ·
NDC 66288-7100
injection, powder, lyophilized, for solution · 1.25 g per 30 mL, 1.5 g per 30 mL, 750 mg per 20 mL ·
NDC 82449-006, 82449-007, 82449-005
injection, powder, lyophilized, for solution, injection · 1 g, 5 g per 100 mL, 10 g per 100 mL, 500 mg ·
NDC 45932-0029, 45932-0032, 45932-0031, 45932-0028
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
injection, powder, lyophilized, for solution · 1 g per 20 mL, 1.25 g per 25 mL, 1.5 g per 30 mL, 1.75 g per 35 mL, 2 g per 40 mL, 5 g per 100 mL ·
NDC 67457-340, 67457-823, 67457-824, 72078-065, 67457-342, 72078-066 and 4 more
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
injection, powder, lyophilized, for solution · 1 g per 20 mL, 5 g per 100 mL ·
NDC 87188-202, 87188-203
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
injection, powder, lyophilized, for solution · 1 g per 20 mL, 1.25 g per 25 mL, 1.5 g per 30 mL, 5 g per 100 mL, 10 g per 100 mL, 500 mg per 10 mL ·
NDC 25021-151, 25021-148, 25021-149, 25021-158, 25021-157, 25021-150 and 1 more
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
Repackaged by
These companies buy Vancomycin in bulk and rebottle it, often for mail-order, clinic or hospital pharmacies. If your bottle shows one of these names, open its NDC to see who made the pills inside.
Recalls
- Aug 6, 2026 · Class II · Baxter Healthcare Corporation · 2 recall notices
CGMP Deviations
- Mar 21, 2024 · Class I · Amneal Pharmaceuticals of New York, LLC
Superpotent Drug: Due to overfilling of drug powder
- Dec 22, 2022 · Class I · Pfizer Inc.
Presence of Particulate Matter: Glass particulate matter detected in injectable.
- Nov 25, 2019 · Class II · AuroMedics Pharma LLC
Discoloration: Product complaints of discoloration after reconstitution of vials.
- Aug 30, 2017 · Class I · Pfizer Inc.
Presence of Particulate Matter: glass particulate found in vial
- Nov 7, 2014 · Class III · Hospira Inc.
Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.
- Oct 6, 2014 · Class II · Hospira Inc. · 2 recall notices
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.