FAMOTIDINE- famotidine injection, solution 
Cantrell Drug Company

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Famotidine 2 mg/mL in 0.9% Sodium Chloride 10 mL Syringe

Label

FAMOTIDINE 
famotidine injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-172
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg  in 1 mL
MANNITOL (UNII: 3OWL53L36A) 4 mg  in 1 mL
ASPARTIC ACID (UNII: 30KYC7MIAI) 0.005 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID (UNII: QTT17582CB)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-172-1210 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/11/2014
Labeler - Cantrell Drug Company (035545763)

Revised: 6/2014
Document Id: 24f07811-6f00-4d0c-8fe1-74ffbc17e404
Set id: 36a915cd-75ae-40b8-b174-026d49ea23d7
Version: 3
Effective Time: 20140616
 
Cantrell Drug Company