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Please see full prescribing and safety information, including boxed warning, for LINCOMYCIN vials.

Available in:

  • 600 mg per 2 mL multi-dose vials
  • 3,000 mg per 10 mL multi-dose vials

Benefits:

  • AP Rated
  • Not made with natural rubber latex

LINCOMYCIN Injection, USP*

Brand Name Equivalent: LINCOCIN® (LINCOCIN is a registered trademark of Pharmacia & Upjohn LLC.)
Therapeutic Category: Anti-Infective

PreventIV Measures® Features:

  • Easy-to-read drug name and dosage strength to aid in identifying the right product
  • Bar codes included on the vial and carton for ease of scanning
  • Unique label design to help products stand out on the shelf
  • Enhanced packaging and labeling designed to promote safety and help reduce the risk of medication errors
NDC
#25021
Description Strength Fill
Volume
Concentration Container
Size
Closure Unit
of Sale
193-02 Glass Vial 600 mg 2 mL 300 mg per mL 2 mL 13 mm 10
193-10 Glass Vial 3,000 mg 10 mL 300 mg per mL 10 mL 13 mm 10

WARNING

Clostridioides difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including lincomycin injection 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. Because lincomycin therapy has been associated with severe colitis which may end fatally, it should be reserved for serious infections where less toxic antimicrobial agents are inappropriate, as described in the INDICATIONS AND USAGE section. It should not be used in patients with nonbacterial infections such as most upper respiratory tract infections. C.diffficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibacterial use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents. If CDAD is suspected or confirmed, ongoing antibacterial use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibacterial treatment of C. difficile, and surgical evaluation should be instituted as clinically indicated.