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Two medicines, side by side

Lincomycin vs ceftriaxone

Lincomycin and ceftriaxone are both labeled for bacterial infections. Drugs@FDA records approvals of lincomycin since 1964 and of ceftriaxone since 1984. Only the lincomycin label carries a boxed warning.

Check it at the source: the lincomycin FDA label on DailyMed (effective March 10, 2025); the ceftriaxone FDA label on DailyMed (effective February 4, 2026).

Highlights of the lincomycin record

Lincomycin (Lincocin) · label of March 10, 2025

Boxed warning

Clostridioides difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including LINCOCIN and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile.

Used for

From the label: indications

LINCOCIN is indicated in the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci. Its use should be reserved for penicillin-allergic patients or other patients for whom, in the judgment of the physician, a penicillin is inappropriate. […]

On the market

Earliest approval on file
December 29, 1964
Generic labelers
8 labelers
Pharmacy cost
Not in the survey

Supply and safety

Shortage
A presentation being discontinued
Recalls
0

Highlights of the ceftriaxone record

Ceftriaxone (Rocephin) · label of February 4, 2026

Used for

From the label: indications

Before instituting treatment with Ceftriaxone for injection, USP, appropriate specimens should be obtained for isolation of the causative organism and for determination of its susceptibility to the drug. Therapy may be instituted prior to obtaining results of susceptibility testing. […]

On the market

Earliest approval on file
December 21, 1984
Generic labelers
16 labelers
Pharmacy cost
$1.44 per vial

Supply and safety

Shortage
No current entry
Recalls
20

Source: FDA drug labels via openFDA (Lincomycin label of March 10, 2025, Ceftriaxone label of February 4, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do lincomycin and ceftriaxone differ on the record?

Only the lincomycin label carries a boxed warning.

How each works, in its label's words: Lincomycin, “Mechanism of Action Lincomycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the bacterial ribosome.”; Ceftriaxone, “Microbiology: Mechanism of Action Ceftriaxone is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis.”

Half-life, in each label's words: Lincomycin, “The biological half-life after intramuscular or intravenous administration is 5.4 ± 1.0 hours.”; Ceftriaxone, “Based on middle ear fluid ceftriaxone concentrations in the 23 to 25 hour and the 46 to 50 hour sampling time …”

Generics: lincomycin since 1991; ceftriaxone since 1987 (Drugs@FDA).

LincomycinCeftriaxone
Labeled forBacterial infectionsUrinary tract infections, Bacterial infections
Pharmacologic classn/aCephalosporin Antibacterial
How it works (label)Mechanism of Action Lincomycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the bacterial ribosome. Lincomycin is predominantly bacteriostatic in vitro.Microbiology: Mechanism of Action Ceftriaxone is a bactericidal agent that acts by inhibition of bacterial cell wall synthesis.
Half-life (label)The biological half-life after intramuscular or intravenous administration is 5.4 ± 1.0 hours.Based on middle ear fluid ceftriaxone concentrations in the 23 to 25 hour and the 46 to 50 hour sampling time intervals, a half-life of 25 hours was calculated.
Earliest approval on file (Drugs@FDA)December 29, 1964December 21, 1984
First generic approvedApril 16, 1991April 30, 1987
Generic labelers (NDC)8 labelers16 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)n/a$1.44 per vial (Ceftriaxone 1 g vial)
12-month price changen/a-4%
Boxed warningYesNo
Shortage nowA presentation being discontinuedNo current entry
Recalls recorded020
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)29338,242
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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