Product NDC: | 41163-127 |
Proprietary Name: | DiBromm |
Non Proprietary Name: | BROMPHENIRAMINE MALEATE,PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 1; 2.5 mg/5mL; mg/5mL & nbsp; BROMPHENIRAMINE MALEATE,PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41163-127 |
Labeler Name: | Equaline |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090513 |
Package NDC: | 41163-127-04 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (41163-127-04) |
NDC Code | 41163-127-04 |
Proprietary Name | DiBromm |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (41163-127-04) |
Product NDC | 41163-127 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BROMPHENIRAMINE MALEATE,PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090513 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Equaline |
Substance Name | BROMPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 1; 2.5 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |