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Chlorhexidine Gluconate - 17856-2002-5 - (Chlorhexidine Gluconate)

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Drug Information of Chlorhexidine Gluconate

Product NDC: 17856-2002
Proprietary Name: Chlorhexidine Gluconate
Non Proprietary Name: Chlorhexidine Gluconate
Active Ingredient(s): .12    mg/mL & nbsp;   Chlorhexidine Gluconate
Administration Route(s): ORAL
Dosage Form(s): RINSE
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorhexidine Gluconate

Product NDC: 17856-2002
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077789
Marketing Category: ANDA
Start Marketing Date: 20090801

Package Information of Chlorhexidine Gluconate

Package NDC: 17856-2002-5
Package Description: 30 mL in 1 CUP, UNIT-DOSE (17856-2002-5)

NDC Information of Chlorhexidine Gluconate

NDC Code 17856-2002-5
Proprietary Name Chlorhexidine Gluconate
Package Description 30 mL in 1 CUP, UNIT-DOSE (17856-2002-5)
Product NDC 17856-2002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Chlorhexidine Gluconate
Dosage Form Name RINSE
Route Name ORAL
Start Marketing Date 20090801
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name CHLORHEXIDINE GLUCONATE
Strength Number .12
Strength Unit mg/mL
Pharmaceutical Classes Decreased Cell Wall Integrity [PE]

Complete Information of Chlorhexidine Gluconate


General Information