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GENTAMICIN SULFATE - 21695-187-05 - (gentamicin sulfate)

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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: 21695-187-05
Package Description: 5 mL in 1 BOTTLE, DROPPER (21695-187-05)

NDC Information of GENTAMICIN SULFATE

NDC Code 21695-187-05
Proprietary Name GENTAMICIN SULFATE
Package Description 5 mL in 1 BOTTLE, DROPPER (21695-187-05)
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]

Complete Information of GENTAMICIN SULFATE


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