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01 3ABRAXIS PHARM
02 1Actavis Inc
03 2Amphastar Pharmaceuticals
04 3Bausch & Lomb Incorporated
05 1Bio Labs
06 3Biotech Laboratories Pty Ltd
07 12Bristol Myers Squibb
08 2Fresenius Kabi USA
09 3Hikma Pharmaceuticals
10 1KIVIPharm
11 3LOCH
12 3Macleods Pharmaceuticals Limited
13 1Montage Laboratories
14 1NUOVO CONSORZIO SANIT.NAZ. Srl
15 2NoroBio Pharmaceutical
16 3Pfizer Inc
17 1Qilu Animal Health Products
18 3Quad Pharma
19 1Reyoung pharmaceutical
20 3Solo Pak
21 2Umedica Laboratories
22 1Warner Chilcott Company, LLC
23 1Zambon Switzerland
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01 3CAPSULE;ORAL
02 3DRY POWDER INJECTION
03 1Dry Powder Injection
04 3INJ
05 33INJECTABLE;INJECTION
06 3INJECTION
07 3Injectable; Injection
08 3Injection
09 1Powder for Injection
10 1Sterilized Injection
11 2Blank
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01 36DISCN
02 9Generic
03 11Blank
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01 2Bio-Kanamycin
02 1Dermaflogil
03 3KANAMYCIN
04 21KANAMYCIN SULFATE
05 12KANTREX
06 3KLEBCIL
07 1Kamacin Ampoule
08 1Kanamycin 1G Biotech
09 1Kanamycin Sulphate
10 1Keimicina
11 2UMEKAN
12 8Blank
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01 5China
02 3India
03 2Italy
04 1Pakistan
05 3South Africa
06 39USA
07 3United Kingdom
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 75MG BASE/2ML
Packaging :
Approval Date : 1984-04-05
Application Number : 62504
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1984-04-05
Application Number : 62504
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1984-04-05
Application Number : 62504
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1985-05-09
Application Number : 62520
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1983-09-30
Application Number : 62466
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1983-09-30
Application Number : 62466
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 60516
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61655
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61655
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 75MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61655
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61901
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61901
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 75MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 61901
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANTREX
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61911
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 75MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62324
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62324
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KANAMYCIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62324
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KLEBCIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 75MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62170
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KLEBCIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 500MG BASE/2ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62170
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KLEBCIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 1GM BASE/3ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62170
Regulatory Info : DISCN
Registration Country : USA