01 1AMANTADINE HYDROCHLORIDE
02 5CHLORHEXIDINE GLUCONATE
03 1CLINDAMYCIN PHOSPHATE
04 2HEXACHLOROPHENE
05 1LACTULOSE
06 1MEGESTROL ACETATE
07 1OXYCODONE HYDROCHLORIDE
08 1PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE
09 1PREDNISONE
01 1AEROSOL, METERED;TOPICAL
02 1AEROSOL;TOPICAL
03 1EMULSION;TOPICAL
04 1SOLUTION;DENTAL
05 3SOLUTION;ORAL
06 4SOLUTION;TOPICAL
07 1SUSPENSION;ORAL
08 2SYRUP;ORAL
01 10.12%
02 110GM/15ML
03 12%
04 12.5%
05 23%
06 24%
07 140MG/ML
08 150MG/5ML
09 25MG/5ML
10 15MG/5ML;6.25MG/5ML
11 1EQ 1% BASE
01 8DISCN
02 3OTC
03 3RX
RLD : No
TE Code : AA
Dosage Form : SYRUP; ORAL
Proprietary Name : AMANTADINE HYDROCHLORIDE
Dosage Strength : 50MG/5ML
Approval Date : 1998-12-24
Application Number : 75060
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
RLD : No
TE Code :
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : EXIDINE
Dosage Strength : 4%
Approval Date : 1984-12-24
Application Number : 19125
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : AEROSOL, METERED; TOPICAL
Proprietary Name : EXIDINE
Dosage Strength : 4%
Approval Date : 1984-12-24
Application Number : 19127
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : EXIDINE
Dosage Strength : 2.5%
Approval Date : 1985-12-17
Application Number : 19421
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : EXIDINE
Dosage Strength : 2%
Approval Date : 1985-12-17
Application Number : 19422
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : No
TE Code : AT
Dosage Form : SOLUTION; DENTAL
Proprietary Name : CHLORHEXIDINE GLUCONATE
Dosage Strength : 0.12%
Approval Date : 2009-06-18
Application Number : 77789
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : No
TE Code :
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : CLINDAMYCIN PHOSPHATE
Dosage Strength : EQ 1% BASE
Approval Date : 1997-07-15
Application Number : 63304
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : AEROSOL; TOPICAL
Proprietary Name : TURGEX
Dosage Strength : 3%
Approval Date : 1982-01-01
Application Number : 18375
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : EMULSION; TOPICAL
Proprietary Name : TURGEX
Dosage Strength : 3%
Approval Date : 1984-11-30
Application Number : 19055
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
Dosage Form : SOLUTION; ORAL
Proprietary Name : LACTULOSE
Dosage Strength : 10GM/15ML
Approval Date : 2002-02-21
Application Number : 75911
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
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