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GOODSENSE LUBRICATING EYE DROPS - 11716-0041-8 - (CARBOXYMETHYLCELLULOSE SODIUM)

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Drug Information of GOODSENSE LUBRICATING EYE DROPS

Product NDC: 11716-0041
Proprietary Name: GOODSENSE LUBRICATING EYE DROPS
Non Proprietary Name: CARBOXYMETHYLCELLULOSE SODIUM
Active Ingredient(s): 5; 9    mg/mL; mg/mL & nbsp;   CARBOXYMETHYLCELLULOSE SODIUM
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of GOODSENSE LUBRICATING EYE DROPS

Product NDC: 11716-0041
Labeler Name: HANLIM PHARM. CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part349
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100730

Package Information of GOODSENSE LUBRICATING EYE DROPS

Package NDC: 11716-0041-8
Package Description: 1 BOTTLE in 1 CARTON (11716-0041-8) > 15 mL in 1 BOTTLE

NDC Information of GOODSENSE LUBRICATING EYE DROPS

NDC Code 11716-0041-8
Proprietary Name GOODSENSE LUBRICATING EYE DROPS
Package Description 1 BOTTLE in 1 CARTON (11716-0041-8) > 15 mL in 1 BOTTLE
Product NDC 11716-0041
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CARBOXYMETHYLCELLULOSE SODIUM
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20100730
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HANLIM PHARM. CO., LTD.
Substance Name CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN
Strength Number 5; 9
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of GOODSENSE LUBRICATING EYE DROPS


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