KEEPAN A - 49873-019-01 - (benzalkonium chloride, lidocaine hydrochloride)

Alphabetical Index


Drug Information of KEEPAN A

Product NDC: 49873-019
Proprietary Name: KEEPAN A
Non Proprietary Name: benzalkonium chloride, lidocaine hydrochloride
Active Ingredient(s): .1; 1    g/100mL; g/100mL & nbsp;   benzalkonium chloride, lidocaine hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of KEEPAN A

Product NDC: 49873-019
Labeler Name: Sato Pharmaceutical Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19810715

Package Information of KEEPAN A

Package NDC: 49873-019-01
Package Description: 1 BOTTLE, SPRAY in 1 CARTON (49873-019-01) > 60 mL in 1 BOTTLE, SPRAY

NDC Information of KEEPAN A

NDC Code 49873-019-01
Proprietary Name KEEPAN A
Package Description 1 BOTTLE, SPRAY in 1 CARTON (49873-019-01) > 60 mL in 1 BOTTLE, SPRAY
Product NDC 49873-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzalkonium chloride, lidocaine hydrochloride
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 19810715
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Sato Pharmaceutical Co., Ltd.
Substance Name BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE
Strength Number .1; 1
Strength Unit g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of KEEPAN A


General Information