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GENTAMICIN SULFATE
GENTAMICIN SULFATE - 21695-187-15 - (gentamicin sulfate)
Drug Information of GENTAMICIN SULFATE
| Product NDC: | 21695-187 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GENTAMICIN SULFATE
| Product NDC: | 21695-187 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062452 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19841010 |
Package Information of GENTAMICIN SULFATE
| Package NDC: | 21695-187-15 |
| Package Description: | 15 mL in 1 BOTTLE, DROPPER (21695-187-15) |
NDC Information of GENTAMICIN SULFATE
| NDC Code | 21695-187-15 |
| Proprietary Name | GENTAMICIN SULFATE |
| Package Description | 15 mL in 1 BOTTLE, DROPPER (21695-187-15) |
| Product NDC | 21695-187 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | gentamicin sulfate |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19841010 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
