01 5AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
02 2DEXMETHYLPHENIDATE HYDROCHLORIDE
03 12LEVOTHYROXINE SODIUM
04 3METHYLPHENIDATE HYDROCHLORIDE
01 22CEDIPROF INC
01 22TABLET;ORAL
01 10.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
02 10.05MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
03 10.075MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
04 10.088MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
05 10.112MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
06 10.125MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
07 10.137MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
08 10.15MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
09 10.175MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
10 10.1MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
11 10.2MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
12 10.3MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium
13 11.25MG;1.25MG;1.25MG;1.25MG
14 210MG
15 12.5MG;2.5MG;2.5MG;2.5MG
16 120MG
17 13.75MG;3.75MG;3.75MG;3.75MG
18 25MG
19 15MG;5MG;5MG;5MG
20 17.5MG;7.5MG;7.5MG;7.5MG
01 22USA
Regulatory Info : DISCN
Registration Country : USA
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET;ORAL
Brand Name : DEXTROAMP SACCHARATE, AMP...
Dosage Strength : 1.25MG;1.25MG;1.25MG;1...
Packaging :
Approval Date : 2022-07-05
Application Number : 210754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET;ORAL
Brand Name : DEXTROAMP SACCHARATE, AMP...
Dosage Strength : 2.5MG;2.5MG;2.5MG;2.5M...
Packaging :
Approval Date : 2022-07-05
Application Number : 210754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET;ORAL
Brand Name : DEXTROAMP SACCHARATE, AMP...
Dosage Strength : 3.75MG;3.75MG;3.75MG;3...
Packaging :
Approval Date : 2022-07-05
Application Number : 210754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET;ORAL
Brand Name : DEXTROAMP SACCHARATE, AMP...
Dosage Strength : 5MG;5MG;5MG;5MG
Packaging :
Approval Date : 2022-07-05
Application Number : 210754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Dosage Form : TABLET;ORAL
Brand Name : DEXTROAMP SACCHARATE, AMP...
Dosage Strength : 7.5MG;7.5MG;7.5MG;7.5M...
Packaging :
Approval Date : 2022-07-05
Application Number : 210754
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DEXMETHYLPHENIDATE HYDROC...
Dosage Strength : 5MG
Packaging :
Approval Date : 2018-09-19
Application Number : 209211
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DEXMETHYLPHENIDATE HYDROC...
Dosage Strength : 10MG
Packaging :
Approval Date : 2018-09-19
Application Number : 209211
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LEVO-T
Dosage Strength : 0.05MG **See current A...
Packaging :
Approval Date : 2002-03-01
Application Number : 21342
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LEVO-T
Dosage Strength : 0.125MG **See current ...
Packaging :
Approval Date : 2002-03-01
Application Number : 21342
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LEVO-T
Dosage Strength : 0.137MG **See current ...
Packaging :
Approval Date : 2003-12-08
Application Number : 21342
Regulatory Info : RX
Registration Country : USA
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