Product NDC: | 64376-612 |
Proprietary Name: | Carbinoxamine Maleate |
Non Proprietary Name: | Carbinoxamine Maleate |
Active Ingredient(s): | 4 mg/5mL & nbsp; Carbinoxamine Maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64376-612 |
Labeler Name: | Boca Pharmacal, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040814 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080226 |
Package NDC: | 64376-612-40 |
Package Description: | 118 mL in 1 BOTTLE (64376-612-40) |
NDC Code | 64376-612-40 |
Proprietary Name | Carbinoxamine Maleate |
Package Description | 118 mL in 1 BOTTLE (64376-612-40) |
Product NDC | 64376-612 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Carbinoxamine Maleate |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20080226 |
Marketing Category Name | ANDA |
Labeler Name | Boca Pharmacal, Inc. |
Substance Name | CARBINOXAMINE MALEATE |
Strength Number | 4 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |