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GENTAMICIN SULFATE
GENTAMICIN SULFATE - 68788-9921-5 - (gentamicin sulfate)
Drug Information of GENTAMICIN SULFATE
| Product NDC: | 68788-9921 |
| Proprietary Name: | GENTAMICIN SULFATE |
| Non Proprietary Name: | gentamicin sulfate |
| Active Ingredient(s): | 3 mg/mL & nbsp; gentamicin sulfate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GENTAMICIN SULFATE
| Product NDC: | 68788-9921 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062452 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120130 |
Package Information of GENTAMICIN SULFATE
| Package NDC: | 68788-9921-5 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (68788-9921-5) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of GENTAMICIN SULFATE
| NDC Code | 68788-9921-5 |
| Proprietary Name | GENTAMICIN SULFATE |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (68788-9921-5) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 68788-9921 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gentamicin sulfate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120130 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
