01 2Actavis Inc
02 1Kolmar Korea Co., Ltd.
03 2Padagis
04 2Sun Pharmaceutical Industries Limited
05 2Taro Pharmaceutical Industries
01 4CREAM;TOPICAL
02 4LOTION;TOPICAL
03 1Solution
01 4DISCN
02 4RX
03 1Blank
01 6AMMONIUM LACTATE
02 1Ascure Lotion
03 2LAC-HYDRIN
01 1South Korea
02 8USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2002-06-11
Application Number : 75575
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2006-02-07
Application Number : 76829
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : South Korea
Brand Name : Ascure Lotion
Dosage Form : Solution
Dosage Strength : 20G
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info : RX
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2004-06-23
Application Number : 75570
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2002-05-01
Application Number : 75774
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LAC-HYDRIN
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1985-04-24
Application Number : 19155
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LAC-HYDRIN
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1996-08-29
Application Number : 20508
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : CREAM;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2003-04-10
Application Number : 75883
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : AMMONIUM LACTATE
Dosage Form : LOTION;TOPICAL
Dosage Strength : EQ 12% BASE
Packaging :
Approval Date : 2004-05-28
Application Number : 76216
Regulatory Info : RX
Registration Country : USA
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