 
                        | Product NDC: | 42254-302 | 
| Proprietary Name: | NEO-POLYCIN | 
| Non Proprietary Name: | NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC | 
| Active Ingredient(s): | 400; 3.5; 10000 U/g; mg/g; U/g & nbsp; NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC | 
| Administration Route(s): | OPHTHALMIC | 
| Dosage Form(s): | OINTMENT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 42254-302 | 
| Labeler Name: | Rebel Distributors Corp | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA060764 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20110715 | 
| Package NDC: | 42254-302-35 | 
| Package Description: | 1 TUBE in 1 CARTON (42254-302-35) > 3.5 g in 1 TUBE | 
| NDC Code | 42254-302-35 | 
| Proprietary Name | NEO-POLYCIN | 
| Package Description | 1 TUBE in 1 CARTON (42254-302-35) > 3.5 g in 1 TUBE | 
| Product NDC | 42254-302 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC | 
| Dosage Form Name | OINTMENT | 
| Route Name | OPHTHALMIC | 
| Start Marketing Date | 20110715 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Rebel Distributors Corp | 
| Substance Name | BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE | 
| Strength Number | 400; 3.5; 10000 | 
| Strength Unit | U/g; mg/g; U/g | 
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Decreased Cell Wall Synthesis & Repair [PE] |