01 1CLEMASTINE FUMARATE
02 1COCAINE HYDROCHLORIDE
03 1GLYCOPYRROLATE
04 2ISONIAZID
05 2ISOSORBIDE MONONITRATE
06 1SODIUM BICARBONATE
01 8OMNIVIUM PHARMS
01 2INJECTABLE;INJECTION
02 1SOLUTION;NASAL
03 5TABLET;ORAL
01 10.2MG/ML
02 1100MG
03 110MG
04 11MEQ/ML
05 12.68MG
06 120MG
07 1300MG
08 14%
01 8USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CLEMASTINE FUMARATE
Dosage Strength : 2.68MG
Packaging :
Approval Date : 1993-10-31
Application Number : 73459
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;NASAL
Brand Name : NUMBRINO
Dosage Strength : 4%
Packaging :
Approval Date : 2020-01-10
Application Number : 209575
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : GLYCOPYRROLATE
Dosage Strength : 0.2MG/ML
Packaging :
Approval Date : 2022-11-29
Application Number : 212871
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ISONIAZID
Dosage Strength : 100MG
Packaging :
Approval Date : 1997-06-26
Application Number : 40090
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ISONIAZID
Dosage Strength : 300MG
Packaging :
Approval Date : 1997-06-26
Application Number : 40090
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : MONOKET
Dosage Strength : 20MG
Packaging :
Approval Date : 1993-06-30
Application Number : 20215
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : MONOKET
Dosage Strength : 10MG
Packaging :
Approval Date : 1993-06-30
Application Number : 20215
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : SODIUM BICARBONATE
Dosage Strength : 1MEQ/ML
Packaging :
Approval Date : 2023-06-15
Application Number : 216364
Regulatory Info : RX
Registration Country : USA
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