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Glycopeptide Antibiotics: Vancomycin, Dalbavancin, Oritavancin and Telavancin by Label

Glycopeptide antibiotics are sugar-carrying peptide rings that kill Gram-positive bacteria. Vancomycin is the original; dalbavancin, oritavancin and telavancin are newer lipoglycopeptides. What each US label states.

A drug class, not one drugFDA-approved membersPrescription antibiotics for Gram-positive infections

Caroline S · Published 2026-11-10

Length

Each is built on a short peptide core, heavily cross-linked into rings and carrying sugars — hence glyco-peptide. Vancomycin hydrochloride is C66H75Cl2N9O24·HCl, molecular weight 1,485.73 (Vancocin label); the label calls it a tricyclic glycopeptide.

Sequence

No simple sequence: the amino acids are unusual, chlorinated and cross-linked into three rings. The newer members add a fatty side chain, which is why their labels call them lipoglycopeptides.

Origin

Vancomycin is made by the soil bacterium Amycolatopsis orientalis (formerly Nocardia orientalis), per the Vancocin label. Dalbavancin, oritavancin and telavancin are semisynthetic: chemically modified natural glycopeptides.

Last reviewed

2026-11-10

What is it good for?

Glycopeptide antibiotics treat infections caused by Gram-positive bacteria, including MRSA. Intravenous vancomycin is used for serious infections; vancomycin swallowed as capsules treats C. difficile diarrhoea because it stays in the gut. The three newer lipoglycopeptides are approved for skin infections, and telavancin also for some hospital pneumonias.

Illustration: A clear glass Erlenmeyer flask with a pale green liquid on a white surface.
Illustration

What the class is

A glycopeptide is a peptide that carries sugar groups. In the antibiotics of this class, the peptide part is a ring of amino acids — many of them unusual, chlorinated or cross-linked — folded into a cup-shaped structure. The Vancocin label describes vancomycin as "a tricyclic glycopeptide antibiotic" made by the soil bacterium Amycolatopsis orientalis, with the formula C66H75Cl2N9O24·HCl.

The newer members add a fatty side chain to that core. Their labels call them lipoglycopeptides. Dalbavancin's label sets out a single-dose regimen, or two doses one week apart, against telavancin's once-daily infusion for 7 to 14 days; how the fatty tail contributes to that difference was not re-read in this run.

Every indication in the table below names Gram-positive bacteria. None of the four labels lists a Gram-negative infection.

The members, by US label

Drug Brand (US) Approved (Drugs@FDA) Type Indication in the label
Vancomycin Vancocin and generics Capsules: 1986-04-15 (NDA 050606) Glycopeptide Oral: C. difficile diarrhoea and staphylococcal enterocolitis; intravenous forms: serious Gram-positive infections
Telavancin Vibativ 2009-09-11 Lipoglycopeptide Complicated skin infections; hospital and ventilator pneumonia caused by S. aureus when alternatives are unsuitable
Dalbavancin Dalvance 2014-05-23 Lipoglycopeptide Acute bacterial skin infections, adults and children
Oritavancin Orbactiv; Kimyrsa 2014-08-06; 2021-03-12 Lipoglycopeptide Acute bacterial skin infections, adults

The table is a census in date order, not a ranking. The labels themselves warn against comparing rates across trials.

Two oritavancin products. Kimyrsa's label states that Orbactiv and Kimyrsa differ in dose strength, infusion time and preparation, and are not interchangeable in how they are made up.

Vancomycin's dates. Drugs@FDA lists the capsule application from 1986, but the drug is much older: a 2006 history in Clinical Infectious Diseases (PMID 16323120) says it became available "more than 50 years ago", fell out of use, and returned as MRSA and C. difficile spread.

What the labels warn about

  • Telavancin (Vibativ) carries a boxed warning: increased mortality among hospital-pneumonia patients with moderate or severe kidney impairment (creatinine clearance 50 mL/min or less), nephrotoxicity, and potential harm to a developing baby.
  • Every label in the class carries the standard antibiotic-stewardship line: use only for infections proven or strongly suspected to be caused by susceptible bacteria.
  • Resistance is part of the class's history. The 2006 review records vancomycin resistance appearing first in enterococci and later in staphylococci.

What is not established here

  • This entry does not compare the members' effectiveness. Their trials were run against different comparators, and choosing an antibiotic is a prescriber's decision.
  • Teicoplanin's approvals outside the US were not checked in this run; only its absence from Drugs@FDA was.
  • The microbiology of each drug was summarised from the class description, not re-read member by member.

Where it stands

Question Answer as of 2026-11-10
Members approved in the US Vancomycin, telavancin, dalbavancin, oritavancin (two products)
Teicoplanin No US application found
Who they treat Gram-positive infections, including MRSA; oral vancomycin for C. difficile
Published record 1,511 PubMed records naming the class; 17 randomised trials
Advice None given here

Other peptide antibiotics in the library work in different ways: daptomycin is a lipopeptide that disrupts bacterial membranes, bacitracin is a cyclic peptide used on the skin, and colistin and polymyxin B act on Gram-negative bacteria, the group glycopeptides cannot reach.

What the research shows

Treat skin and skin-structure infections

FDA-approved indications of dalbavancin (Dalvance), oritavancin (Orbactiv, Kimyrsa) and telavancin (Vibativ), each label citing its randomised trials

Oral vancomycin treats C. difficile-associated diarrhoea

Vancocin capsule label: indicated for C. difficile-associated diarrhoea; the label states that oral vancomycin is not effective for other infections and that intravenous vancomycin is not effective for this one

Kill bacteria by blocking cell-wall building

Class mechanism described in the labels' microbiology sections and in reviews; not re-opened for each member in this run

Bars show how much of the evidence is in humans, not how well anything works.

Where it stands

United States

Vancomycin (Vancocin capsules NDA 050606, original approval 1986-04-15 in Drugs@FDA; many generics) · telavancin (Vibativ, NDA 022110, 2009-09-11) · dalbavancin (Dalvance, NDA 021883, 2014-05-23) · oritavancin (Orbactiv, NDA 206334, 2014-08-06; Kimyrsa, NDA 214155, 2021-03-12).

Teicoplanin

No teicoplanin application was found in Drugs@FDA (openFDA query, 2026-11-10). It is used in other countries; its status there was not checked in this run.

Published record

PubMed: 1,511 records use 'glycopeptide antibiotic(s)' in the title or abstract; 17 of them are randomised controlled trials (2026-11-10).

Frequently asked questions

What are glycopeptide antibiotics?

They are antibiotics built from a ring of amino acids that carries sugar groups. Vancomycin is the best known. They act on Gram-positive bacteria, such as Staphylococcus aureus, including MRSA.

Is vancomycin a peptide?

Yes, in structure: it is a glycopeptide, a cross-linked ring of amino acids with sugars attached. Its label calls it a tricyclic glycopeptide antibiotic.

What is a lipoglycopeptide?

A glycopeptide with a fatty side chain added. Dalbavancin, oritavancin and telavancin are the three approved in the US; their labels use the word lipoglycopeptide.

Which glycopeptide antibiotics are approved in the US?

Vancomycin, telavancin (Vibativ, 2009), dalbavancin (Dalvance, 2014) and oritavancin (Orbactiv, 2014, and Kimyrsa, 2021), per Drugs@FDA. No teicoplanin application was found.

Why is oral vancomycin used for C. difficile?

Swallowed vancomycin is barely absorbed, so it stays in the gut where C. difficile grows. For the same reason the label says oral vancomycin does not treat infections elsewhere in the body. Treatment choices belong with the prescriber.