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Bromfed
Bromfed - 60432-837-15 - (Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide)
Drug Information of Bromfed
| Product NDC: | 60432-837 |
| Proprietary Name: | Bromfed |
| Non Proprietary Name: | Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 2; 10; 30 mg/5mL; mg/5mL; mg/5mL & nbsp; Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bromfed
| Product NDC: | 60432-837 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088811 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090821 |
Package Information of Bromfed
| Package NDC: | 60432-837-15 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (60432-837-15) |
NDC Information of Bromfed
| NDC Code | 60432-837-15 |
| Proprietary Name | Bromfed |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (60432-837-15) |
| Product NDC | 60432-837 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20090821 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 2; 10; 30 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes | Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC],Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],Sigma-1 Agonist [EPC],Uncompetitive NMDA Receptor Antagonists [MoA],Sigma-1 Receptor Agonists [MoA] |
