01 1ALRA
02 1ANHUI ANKE BIOTECHNOLOGY (GROUP) CO., LTD
03 3ANI Pharmaceuticals Inc
04 2Actavis Inc
05 4Alphapharm PTY Ltd
06 2Amneal Pharmaceuticals
07 4Arbor Pharmaceuticals
08 1Aurobindo Pharma Limited
09 8Azurity Pharma
10 2Barr Laboratories
11 2Bausch & Lomb Incorporated
12 2Celogen Pharma Pvt. Ltd
13 2ENDO OPERATIONS
14 2Eli Lilly
15 1Infugen Pharma
16 3Meda AB
17 1NASKA
18 4Pfizer Inc
19 4Ross Lab
20 1Umedica Laboratories
21 2Varichem Pharmaceuticals Pvt Ltd
22 2Wyeth Pharmaceuticals Inc
23 2Zim Laboratories
24 2Zydus Lifesciences
01 2GRANULAT TILL ORAL SUSPENSION
02 1GRANULAT TILL ORAL SUSPENSION I DOSPÅSE
03 16GRANULE;ORAL
04 2GRANULES FOR SUSPENSION
05 1Oral Powder for Reconstitution
06 1Oral Suspension
07 1SACHET
08 1SUSPENSION/DROPS;ORAL
09 17SUSPENSION;ORAL
10 3TABLET, CHEWABLE;ORAL
11 5TABLET;ORAL
12 2Tablet
13 2Taste Masked Granules for Oral Suspension
14 4Blank
01 30DISCN
02 3Generic
03 12RX
04 13Blank
01 2E-MYCIN E
02 2E-Mycin 200
03 2E-Mycin 400
04 2E.E.S.
05 1E.E.S. 200
06 3E.E.S. 400
07 3ERYPED
08 21ERYTHROMYCIN ETHYLSUCCINATE
09 1ERYTHROMYCIN ETHYLSUCCINATE AND SULFISOXAZOLE ACETYL
10 1ERYZOLE
11 3Ery-Max
12 2Etrocin
13 4PEDIAMYCIN
14 1PEDIAMYCIN 400
15 1PEDIAZOLE
16 1UTHROCIN
17 2WYAMYCIN E
18 6Blank
01 4Australia
02 1China
03 6India
04 3Sweden
05 42USA
06 2Zimbabwe
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62055
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 400MG BASE/5ML
Packaging :
Approval Date : 2018-11-02
Application Number : 62055
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 2018-11-02
Application Number : 62055
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E.E.S. 200
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 61639
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E.E.S. 400
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 400MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 61639
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : E.E.S.
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50207
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYPED
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 400MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50207
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYPED
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1987-03-30
Application Number : 50207
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E.E.S.
Dosage Form : TABLET, CHEWABLE;ORAL
Dosage Strength : EQ 200MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50297
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ERYPED
Dosage Form : TABLET, CHEWABLE;ORAL
Dosage Strength : EQ 200MG BASE
Packaging :
Approval Date : 1988-07-05
Application Number : 50297
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61904
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E.E.S. 400
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 61905
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : E.E.S. 400
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 400MG BASE
Packaging :
Approval Date : 1982-08-12
Application Number : 61905
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62177
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ERYTHROMYCIN ETHYLSUCCINATE
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 400MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62177
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E-MYCIN E
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62198
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : E-MYCIN E
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 400MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62198
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ERYTHROMYCIN ETHYLSUCCINATE; SULFISOXAZOLE ACETYL
Brand Name : PEDIAZOLE
Dosage Form : GRANULE;ORAL
Dosage Strength : EQ 200MG BASE/5ML;EQ 600MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50529
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : WYAMYCIN E
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 400MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62123
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : WYAMYCIN E
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 200MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 62123
Regulatory Info : DISCN
Registration Country : USA
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