NDC Code |
21695-438-10 |
Proprietary Name |
Neomycin and Polymyxin B Sulfates and Hydrocortisone |
Package Description |
1 BOTTLE, DROPPER in 1 CARTON (21695-438-10) > 10 mL in 1 BOTTLE, DROPPER |
Product NDC |
21695-438 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone |
Dosage Form Name |
SUSPENSION/ DROPS |
Route Name |
AURICULAR (OTIC) |
Start Marketing Date |
19951229 |
Marketing Category Name |
ANDA |
Labeler Name |
Rebel Distributors Corp |
Substance Name |
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
Strength Number |
10; 3.5; 10000 |
Strength Unit |
mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |