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GENTAMICIN SULFATE
GENTAMICIN SULFATE - 48102-102-35 - (GENTAMICIN SULFATE)
Drug Information of GENTAMICIN SULFATE
| Product NDC: | 48102-102 |
| Proprietary Name: | GENTAMICIN SULFATE |
| Non Proprietary Name: | GENTAMICIN SULFATE |
| Active Ingredient(s): | 3 mg/g & nbsp; GENTAMICIN SULFATE |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GENTAMICIN SULFATE
| Product NDC: | 48102-102 |
| Labeler Name: | Fera Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065024 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110103 |
Package Information of GENTAMICIN SULFATE
| Package NDC: | 48102-102-35 |
| Package Description: | 1 TUBE in 1 CARTON (48102-102-35) > 3.5 g in 1 TUBE |
NDC Information of GENTAMICIN SULFATE
| NDC Code | 48102-102-35 |
| Proprietary Name | GENTAMICIN SULFATE |
| Package Description | 1 TUBE in 1 CARTON (48102-102-35) > 3.5 g in 1 TUBE |
| Product NDC | 48102-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GENTAMICIN SULFATE |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110103 |
| Marketing Category Name | ANDA |
| Labeler Name | Fera Pharmaceuticals, LLC |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
