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banophen
banophen - 0904-1228-20 - (Diphenhydramine HCl)
Drug Information of banophen
| Product NDC: | 0904-1228 |
| Proprietary Name: | banophen |
| Non Proprietary Name: | Diphenhydramine HCl |
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; Diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of banophen
| Product NDC: | 0904-1228 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19901215 |
Package Information of banophen
| Package NDC: | 0904-1228-20 |
| Package Description: | 1 BOTTLE in 1 CARTON (0904-1228-20) > 118 mL in 1 BOTTLE |
NDC Information of banophen
| NDC Code | 0904-1228-20 |
| Proprietary Name | banophen |
| Package Description | 1 BOTTLE in 1 CARTON (0904-1228-20) > 118 mL in 1 BOTTLE |
| Product NDC | 0904-1228 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19901215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
